Capecitabine by Chartwell RX, LLC CAPECITABINE tablet

Capecitabine by

Drug Labeling and Warnings

Capecitabine by is a Prescription medication manufactured, distributed, or labeled by Chartwell RX, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • BOXED WARNING (What is this?)

    WARNING: INCREASED RISK OF BLEEDING WITH CONCOMITANT USE OF VITAMIN K ANTAGONISTS

    Altered coagulation parameters and/or bleeding, including death, have been reported in patients taking capecitabine concomitantly with oral vitamin K antagonists, such as warfarin [see Warnings and Precautions (5.1), Drug Interactions (7.2)].

    Clinically significant increases in prothrombin time (PT) and international normalized ratio (INR) have been reported in patients who were on stable doses of a vitamin K antagonist at the time capecitabine was introduced. These events occurred within several days and up to several months after initiating capecitabine and, in a few cases, within 1 month after stopping capecitabine. These events occurred in patients with and without liver metastases.

    Monitor INR more frequently and adjust the dose of the vitamin K antagonist as appropriate [see Drug Interactions (7.2)].

  • 1 INDICATIONS AND USAGE

    1.1 Colorectal Cancer

    Capecitabine is indicated for the:

    • adjuvant treatment of patients with Stage III colon cancer as a single agent or as a component of a combination chemotherapy regimen.
    • perioperative treatment of adults with locally advanced rectal cancer as a component of chemoradiotherapy.
    • treatment of patients with unresectable or metastatic colorectal cancer as a single agent or as a component of a combination chemotherapy regimen.

    1.2 Breast Cancer

    Capecitabine is indicated for the:

    • treatment of patients with advanced or metastatic breast cancer as a single agent if an anthracycline- or taxane-containing chemotherapy is not indicated.
    • treatment of patients with advanced or metastatic breast cancer in combination with docetaxel after disease progression on prior anthracycline-containing chemotherapy.

    1.3 Gastric, Esophageal, or Gastroesophageal Junction Cancer 

    Capecitabine is indicated for the:

    • treatment of adults with unresectable or metastatic gastric, esophageal, or gastroesophageal junction cancer as a component of a combination chemotherapy regimen.
    • treatment of adults with HER2-overexpressing metastatic gastric or gastroesophageal junction adenocarcinoma who have not received prior treatment for metastatic disease as a component of a combination regimen.

    1.4 Pancreatic Cancer

    Capecitabine is indicated for the adjuvant treatment of adults with pancreatic adenocarcinoma as a component of a combination chemotherapy regimen.

  • 2 DOSAGE AND ADMINISTRATION

    2.1 Recommended Dosage for Colorectal Cancer

    Adjuvant Treatment of Colon Cancer

    Single Agent

    The recommended dosage of capecitabine is 1,250 mg/m 2orally twice daily for the first 14 days of each 21-day cycle for a maximum of 8 cycles.

    In Combination with Oxaliplatin-Containing Regimens

    The recommended dosage of capecitabine is 1,000 mg/m 2orally twice daily for the first 14 days of each 21-day cycle for a maximum of 8 cycles in combination with oxaliplatin 130 mg/m 2administered intravenously on day 1 of each cycle.

    Refer to the oxaliplatin prescribing information for additional dosing information as appropriate.

    Perioperative Treatment of Rectal Cancer

    The recommended dosage of capecitabine is 825 mg/m 2orally twice daily when administered with concomitant radiation therapy and 1,250 mg/m 2orally twice daily when administered without radiation therapy as part of a peri-operative combination regimen.

    Unresectable or Metastatic Colorectal Cancer

    Single Agent

    The recommended dosage of capecitabine is 1,250 mg/m 2orally twice daily for the first 14 days of a 21-day cycle until disease progression or unacceptable toxicity.

    In Combination with Oxaliplatin

    The recommended dosage of capecitabine is 1,000 mg/m 2orally twice daily for the first 14 days of each 21-day cycle until disease progression or unacceptable toxicity in combination with oxaliplatin 130 mg/m 2administered intravenously on day 1 of each cycle.
    Refer to the Prescribing Information for oxaliplatin for additional dosing information as appropriate.

    2.2 Recommended Dosage for Breast Cancer

    Advanced or Metastatic Breast Cancer

    Single Agent

    The recommended dosage of capecitabine is 1,000 mg/m 2or 1,250 mg/m 2orally twice daily for the first 14 days of a 21-day cycle until disease progression or unacceptable toxicity. Individualize the dose and dosing schedule of capecitabine based on patient risk factors and adverse reactions.

    In Combination with Docetaxel

    The recommended dosage of capecitabine is 1,000 mg/m 2or 1,250 mg/m 2orally twice daily for the first 14 days of a 21-day cycle until disease progression or unacceptable toxicity in combination with docetaxel 75 mg/m 2administered intravenously on day 1 of each cycle.

    Refer to the Prescribing Information for docetaxel for additional dosing information as appropriate.

    2.3 Recommended Dosage for Gastric, Esophageal, or Gastroesophageal Junction Cancer

    The recommended dosage of capecitabine for unresectable or metastatic gastric, esophageal, or gastroesophageal junction cancer is:

    • 625 mg/m 2orally twice daily on days 1 to 21 of each 21-day cycle for a maximum of 8 cycles in combination with platinum-containing chemotherapy.
      OR
    • 850 mg/m 2or 1,000 mg/m 2orally twice daily for the first 14 days of each 21-day cycle until disease progression or unacceptable toxicity in combination with oxaliplatin 130 mg/m 2administered intravenously on day 1 of each cycle. Individualize the dose and dosing schedule of capecitabine based on patient risk factors and adverse reactions.

    The recommended dosage of capecitabine for HER2-overexpressing metastatic gastric or gastroesophageal junction adenocarcinoma is 1,000 mg/m 2orally twice daily for the first 14 days of each 21-day cycle until disease progression or unacceptable toxicity in combination with cisplatin and trastuzumab.

    Refer to the Prescribing Information for agents used in combination for additional dosing information as appropriate.

    2.4 Recommended Dosage for Pancreatic Cancer

    The recommended dosage of capecitabine is 830 mg/m 2orally twice daily for the first 21 days of each 28-day cycle until disease progression, unacceptable toxicity, or for a maximum 6 cycles in combination with gemcitabine 1,000 mg/m 2administered intravenously on days 1, 8, and 15 of each cycle.
    Refer to Prescribing Information for gemcitabine for additional dosing information as appropriate.

    2.5 Dosage Modifications for Adverse Reactions

    Monitor patients for adverse reactions and modify dosages of capecitabine as described in Table 1.

    Do not replace missed doses of capecitabine; instead resume capecitabine with the next planned dosage.

    When capecitabine is administered with docetaxel, withhold capecitabine and docetaxel until the requirements for resuming both capecitabine and docetaxel are met. Refer to the Prescribing Information for docetaxel for additional dosing information as appropriate.

    Table 1 Recommended Dosage Modifications for Adverse Reactions

    SeverityDosage ModificationResume at Same or Reduced Dose (Percent of Current Dose)
    Grade 2
    1 st  appearance
    Withhold until resolved to grade 0-1.     		100%
    2 nd  appearance 75%
    3 rd  appearance 50%
    4 thappearance Permanently discontinue.-
    Grade 3
    1 st  appearance Withhold until resolved to grade 0-1.75%
    2 ndappearance 50%
    3 rd  appearance Permanently discontinue.-
    Grade 4

    1 stappearance     		Permanently discontinue OR Withhold until resolved to grade 0-1.50%

     Hyperbilirubinemia

    Patients with Grade 3-4 hyperbilirubinemia may resume treatment once the event is Grade 2 or less (less than three times the upper limit of normal), using the percent of current dose as shown in column 3 of Table 1 [see Warnings and Precautions (5.10)].

    2.6 Dosage Modification For Renal Impairment

    Reduce the dose of capecitabine by 25% for patients with creatinine clearance (CLcr) of 30 to 50 mL/min as determined by Cockcroft-Gault equation. A dosage has not been established in patients with severe renal impairment (CLcr <30 mL/min) [ see Use in Specific Populations (8.6)].

    2.7 Administration

    Round the recommended dosage for patients to the nearest 150 mg dose to provide whole capecitabine tablets.

    Swallow capecitabine tablets whole with water within 30 minutes after a meal. Do not chew, cut, or crush capecitabine tablets [see Warnings and Precautions (5.12)].

    Take capecitabine at the same time each day approximately 12 hours apart.

    Do not take an additional dose after vomiting and continue with the next scheduled dose.

    Do not take a missed dose and continue with the next scheduled dose.

    Capecitabine is a hazardous drug. Follow applicable special handling and disposal procedures. 1

  • 3 DOSAGE FORMS AND STRENGTHS

    Tablets, film-coated:

    • 150 mg: biconvex, oblong, light-peach colored, with C150 on one side and plain on the  other
    • 500 mg: biconvex, oblong, peach colored, with C500 on one side and plain on the other 
  • 4 CONTRAINDICATIONS

    Capecitabine is contraindicated in patients with history of severe hypersensitivity reaction to fluorouracil or capecitabine [ see Adverse Reactions (6.1)] .

  • 5 WARNINGS AND PRECAUTIONS

    5.1 Increased Risk of Bleeding With Concomitant Use of Vitamin K Antagonists

    Altered coagulation parameters and/or bleeding, including death, have been reported in patients taking capecitabine concomitantly with vitamin K antagonists, such as warfarin.
    Clinically significant increases in PT and INR have been reported in patients who were on stable doses of oral vitamin K antagonists at the time capecitabine was introduced. These events occurred within several days and up to several months after initiating capecitabine and, in a few cases, within 1 month after stopping capecitabine. These events occurred in patients with and without liver metastases.
    Monitor INR more frequently and adjust the dose of the vitamin K antagonist as appropriate [ see Drug Interactions (7.1)].

    5.2 Serious Adverse Reactions from Dihydropyrimidine Dehydrogenase (DPD) Deficiency

    Patients with certain homozygous or compound heterozygous variants in the DPYD gene known to result in complete or near complete absence of DPD activity (complete DPD deficiency) are at increased risk for acute early-onset toxicity and serious, including fatal, adverse reactions due to capecitabine (e.g., mucositis, diarrhea, neutropenia, and neurotoxicity). Patients with partial DPD activity (partial DPD deficiency) may also have increased risk of serious, including fatal, adverse reactions.

    Capecitabine is not recommended for use in patients known to have certain homozygous or compound heterozygous DPYD variants that result in complete DPD deficiency.

    Withhold or permanently discontinue capecitabine based on clinical assessment of the onset, duration, and severity of the observed adverse reactions in patients with evidence of acute early onset or unusually severe reactions, which may indicate complete DPD deficiency. No capecitabine dose has been proven safe for patients with complete DPD deficiency. There are insufficient data to recommend a specific dose in patients with partial DPD deficiency.
    Consider testing for genetic variants of DPYD prior to initiating capecitabine to reduce the risk of serious adverse reactions if the patient’s clinical status permits and based on clinical judgement [see Clinical Pharmacology (12.5)]. Serious adverse reactions may still occur even if no DPYD variants are identified.
    An FDA-authorized test for the detection of genetic variants of DPYD to identify patients at risk of serious adverse reactions due to increased systemic exposure to capecitabine is not currently available. Currently available tests used to identify DPYD variants may vary in accuracy and design (e.g., which DPYD variant(s) they identify).

    5.3 Cardiotoxicity

    Cardiotoxicity can occur with capecitabine. Myocardial infarction/ischemia, angina, dysrhythmias, cardiac arrest, cardiac failure, sudden death, electrocardiographic changes, and cardiomyopathy have been reported with capecitabine. These adverse reactions may be more common in patients with a prior history of coronary artery disease.
    Withhold capecitabine for cardiotoxicity as appropriate [ see Dosage and Administration (2.5)]. The safety of resumption of capecitabine in patients with cardiotoxicity that has resolved have not been established.

    5.4 Diarrhea

    Diarrhea, sometimes severe, can occur with capecitabine. In 875 patients with metastatic breast or colorectal cancer who received capecitabine as a single agent, the median time to first occurrence of grade 2 to 4 diarrhea was 34 days (range: 1 day to 1 year). The median duration of grade 3 to 4 diarrhea was 5 days.
    Withhold capecitabine and then resume at same or reduced dose or permanently discontinue based on severity and occurrence [see Dosage and Administration (2.5)].

    5.5 Dehydration

    Dehydration can occur with capecitabine. Patients with anorexia, asthenia, nausea, vomiting, or diarrhea may be at an increased risk of developing dehydration with capecitabine. Optimize hydration before starting capecitabine. Monitor hydration status and kidney function at baseline and as clinically indicated. Withhold capecitabine and then resume at same or reduced dose, or permanently discontinue, based on severity and occurrence [see Dosage and Administration (2.5)].

    5.6 Renal Toxicity

    Serious renal failure, sometimes fatal, can occur with capecitabine. Renal impairment or coadministration of capecitabine with other products known to cause renal toxicity may increase the risk of renal toxicity [see Drug Interactions (7.3)].

    Monitor renal function at baseline and as clinically indicated. Optimize hydration before starting capecitabine. Withhold capecitabine and then resume at same or reduced dose, or permanently discontinue, based on severity and occurrence [see Dosage and Administration (2.5)].

    5.7 Serious Skin Toxicities

    Severe cutaneous adverse reactions (SCARs), including Stevens-Johnson Syndrome and toxic epidermal necrolysis (TEN), which can be fatal, can occur with capecitabine [ see Adverse Reactions (6.2)].
    Monitor for new or worsening serious skin reactions. Permanently discontinue capecitabine for severe cutaneous adverse reactions.

    5.8 Palmar-Plantar Erythrodysesthesia Syndrome

    Palmar-plantar erythrodysesthesia syndrome (PPES) can occur with capecitabine.
    In patients with metastatic breast or colorectal cancer who received capecitabine as a single agent, the median time to onset of grades 1 to 3 PPES was 2.6 months (range: 11 days to 1 year).
    Withhold capecitabine and then resume at same or reduced dose or permanently discontinue based on severity and occurrence [see Dosage and Administration (2.5)].

    5.9 Myelosuppression

    Myelosuppression can occur with capecitabine.
    In the 875 patients with metastatic breast or colorectal cancer who received capecitabine as a single agent, 3.2% had grade 3 or 4 neutropenia, 1.7% had grade 3 or 4 thrombocytopenia, and 2.4% had grade 3 or 4 anemia.
    In the 251 patients with metastatic breast cancer who received capecitabine with docetaxel, 68% had grade 3 or 4 neutropenia, 2.8% had grade 3 or 4 thrombocytopenia, and 10% had grade 3 or 4 anemia.
    Necrotizing enterocolitis (typhlitis) has been reported. Consider typhlitis in patients with fever, neutropenia and abdominal pain.
    Monitor complete blood count at baseline and before each cycle. Capecitabine is not recommended if baseline neutrophil count <1.5 x 10 9/L or platelet count <100 x 10 9/L. For grade 3 to 4 myelosuppression, withhold capecitabine and then resume at same or reduced dose, or permanently discontinue, based on occurrence [ see Dosage and Administration (2.5)].

    5.10 Hyperbilirubinemia

    Hyperbilirubinemia can occur with capecitabine. In the 875 patients with metastatic breast or colorectal cancer who received capecitabine as a single agent, grade 3 hyperbilirubinemia occurred in 15% of patients and grade 4 hyperbilirubinemia occurred in 3.9%. Of the 566 patients who had hepatic metastases at baseline and the 309 patients without hepatic metastases at baseline, grade 3 or 4 hyperbilirubinemia occurred in 23% and 12%, respectively. Of these 167 patients with grade 3 or 4 hyperbilirubinemia, 19% had postbaseline increased alkaline phosphatase and 28% had postbaseline increased transaminases at any time (not necessarily concurrent). The majority of these patients with increased transaminases or alkaline phosphatase had liver metastases at baseline. In addition, 58% and 35% of the 167 patients with grade 3 or 4 hyperbilirubinemia had pre- and postbaseline increased alkaline phosphatase or transaminases (grades 1 to 4), respectively. Only 8% (n=13) and 3% (n=5) had grade 3 or 4 increased alkaline phosphatase or transaminases.
    In the 596 patients who received capecitabine for metastatic colorectal cancer, the incidence of grade 3 or 4 hyperbilirubinemia was similar to that observed for the pooled population of patients with metastatic breast and colorectal cancer. The median time to onset for grade 3 or 4 hyperbilirubinemia was 64 days and median total bilirubin increased from 8 µm/L at baseline to 13 µm/L during treatment with capecitabine. Of the 136 patients with grade 3 or 4 hyperbilirubinemia, 49 patients had grade 3 or 4 hyperbilirubinemia as their last measured value, of which 46 had liver metastases at baseline.
    In the 251 patients with metastatic breast cancer who received capecitabine with docetaxel, grade 3 hyperbilirubinemia occurred in 7% and grade 4 hyperbilirubinemia occurred in 2%.
    Withhold capecitabine and then resume at a same or reduced dose, or permanently discontinue, based on occurrence [see Dosage and Administration (2.5)]. Patients with Grade 3-4 hyperbilirubinemia may resume treatment once the event is Grade 2 or less than three times the upper limit of normal, using the percent of current dose as shown in Table 1 [see Dosage and Administration (2.5)].

    5.11 Embryo-Fetal Toxicity

    Based on findings from animal reproduction studies and its mechanism of action, capecitabine can cause fetal harm when administered to a pregnant woman. Insufficient data is available on capecitabine use in pregnant women to evaluate a drug-associated risk. In animal reproduction studies, administration of capecitabine to pregnant animals during the period of organogenesis caused embryo lethality and teratogenicity in mice and embryo lethality in monkeys at 0.2 and 0.6 times the human exposure (AUC) in patients who received a dosage of 1,250 mg/m 2twice daily, respectively.
    Advise pregnant women of the potential risk to a fetus. Advise females of reproductive potential to use effective contraception during treatment with capecitabine and for 6 months following the last dose. Advise males with female partners of reproductive potential to use effective contraception during treatment with capecitabine and for 3 months following the last dose [ see Use in Specific Populations (8.1, 8.3)].

    5.12 Eye Irritation, Skin Rash, and Other Adverse Reactions from Exposure to Crushed Tablets

    In instances of exposure to crushed capecitabine tablets, the following adverse reactions have been reported: eye irritation and swelling, skin rash, diarrhea, paresthesia, headache, gastric irritation, vomiting and nausea. Advise patients not to cut or crush tablets.
    If capecitabine tablets must be cut or crushed, this should be done by a professional trained in safe handling of cytotoxic drugs using appropriate equipment and safety procedures [see Dosage and Administration (2.7)]. The safety and effectiveness have not been established for the administration of crushed capecitabine tablets.

  • 6 ADVERSE REACTIONS

    The following clinically significant adverse reactions are described elsewhere in the labeling:

    6.1 Clinical Trials Experience

    Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.

    Adjuvant Treatment of Colon Cancer

    Single Agent

    The safety of capecitabine as a single agent was evaluated in patients with Stage III colon cancer in X-ACT [ see Clinical Studies (14.1)]. Patients received capecitabine 1,250 mg/m 2orally twice daily for the first 14 days of a 21-day cycle (N=995) or leucovorin 20 mg/m 2intravenously followed by fluorouracil 425 mg/m 2as an intravenous bolus on days 1 to 5 of each 28-day cycle (N=974). Among patients who received capecitabine, the median duration of treatment was 5.4 months.

    Deaths due to all causes occurred in 0.8% of patients who received capecitabine on study or within 28 days of receiving study drug. Permanent discontinuation due to an adverse reaction occurred in 11% of patients who received capecitabine.

    Most common adverse reactions (>30%) were palmar-plantar erythrodysesthesia syndrome, diarrhea, and nausea.

    Tables 2 and 3 summarize the adverse reactions and laboratory abnormalities in X-ACT.


    Table 2 Adverse Reactions (>10%) in Patients Who Received Capecitabine for Adjuvant Treatment of
    Colon Cancer in X-ACT

    Adverse Reaction
    Capecitabine (N=995)
    Fluorouracil + Leucovorin (N=974)

    All Grades (%)

    Grade 3 or 4 (%)

    All Grades (%)
    Grade 3 or 4 (%)
    Skin and Subcutaneous Tissue

    Palmar-plantar erythrodysesthesia syndrome
    60
    17
    9
    <1

    Gastrointestinal

    Diarrhea
    47
    12
    65
    14

    Nausea
    34
    2
    47
    2

    Stomatitis
    22
    2
    60
    14

    Vomiting
    15
    2
    21
    2

    Abdominal pain
    14
    3
    16
    2

    General

    Fatigue
    16
    <1
    16
    1

    Asthenia
    10
    <1
    10
    1

    Lethargy
    10
    <1
    9
    <1

    Clinically relevant adverse reactions in <10% of patients are presented below:

    Eye:conjunctivitis

    Gastrointestinal:constipation, upper abdominal pain, dyspepsia

    General:pyrexia

    Metabolism and Nutrition:anorexia

    Nervous System:dizziness, dysgeusia, headache

    Skin & Subcutaneous Tissue:rash, alopecia, erythema

    Table 3 Grade 3 or 4 Laboratory Abnormalities (>1%) in Patients Who Received Capecitabine as a
    Single Agent for Adjuvant Treatment of Colon Cancer in XACT


    Laboratory Abnormality
    Capecitabine (N=995)
    Fluorouracil + Leucovorin (N=974)

    Grade 3 or 4 (%)
    Grade 3 or 4 (%)

    Bilirubin increased
    20
    6

    Lymphocytes decreased
    13
    13

    Neutrophils/granulocytes decreased
    2.4
    26

    Calcium decreased
    2.3
    2.2

    Neutrophils decreased
    2.2
    26

    ALT increased
    1.6
    0.6

    Calcium increased
    1.1
    0.7

    Hemoglobin decreased
    1
    1.2

    Platelets decreased
    1
    0.7

    In Combination with Oxaliplatin-Containing Regimens

    The safety of capecitabine for the perioperative treatment of adults with Stage III colon cancer as a component of a combination chemotherapy regimen was derived from published literature [see Clinical Studies (14.1)]. The safety of capecitabine for the adjuvant treatment of patients with Stage III colon cancer as a component of a combination chemotherapy regimen was similar to those in patients treated with capecitabine as a single agent, with the exception of an increased incidence of neurosensory toxicity.

    Perioperative Treatment of Rectal Cancer

    The safety of capecitabine for the perioperative treatment of adults with locally advanced rectal cancer as a component of chemoradiotherapy was derived from published literature [see Clinical Studies (14.1)]. The safety of capecitabine for the perioperative treatment of adults with locally advanced rectal cancer as a component of chemoradiotherapy was similar to those in patients treated with capecitabine as a single agent, with the exception of an increased incidence of diarrhea.

    Metastatic Colorectal Cancer

    Single Agent

    The safety of capecitabine as a single agent was evaluated in a pooled metastatic colorectal cancer population (Study SO14695 and Study SO14796) [ see Clinical Studies (14.1)]. Patients received capecitabine 1,250 mg/m 2orally twice a day for the first 14 days of a 21-day cycle (N=596) or leucovorin 20 mg/m 2intravenously followed by fluorouracil 425 mg/m 2as an intravenous bolus on days 1 to 5 of each 28-day cycle (N=593). Among the patients who received capecitabine, the median duration of treatment was 4.6 months.

    Deaths due to all causes occurred in 8% of patients who received capecitabine on study or within 28 days of receiving study drug. Permanent discontinuation due to an adverse reaction or intercurrent illness occurred in 13% of patients who received capecitabine.

    Most common adverse reactions (>30%) were anemia, diarrhea, palmar-plantar erythrodysesthesia syndrome, hyperbilirubinemia, nausea, fatigue, and abdominal pain.

    Table 4 shows the adverse reactions occurring in this pooled colorectal cancer population.


    Table 4 Adverse Reactions (>10%) in Patients Who Received Capecitabine in Pooled Metastatic
    Colorectal Cancer Population (Study SO14695 and Study SO14796)


    Adverse Reaction

    Capecitabine (N=596)

    Fluorouracil + Leucovorin (N=593)


    All Grades (%)

    Grade 3 (%)

    Grade 4 (%)

    All Grades (%)

    Grade 3 (%)
    G rade 4 (%)

    Blood and Lymphatic System

    Anemia
    80
    2
    <1
    79
    1
    <1

    Neutropenia
    13
    1
    2
    46
    8
    13

    Gastrointestinal

    Diarrhea
    55
    13
    2
    61
    10
    2

    Nausea
    43
    4
    -
    51
    3
    <1

    Abdominal pain
    35
    9
    <1
    31
    5
    -

    Vomiting
    27
    4
    <1
    30
    4
    <1

    Stomatitis
    25
    2
    <1
    62
    14
    1

    Constipation
    14
    1
    <1
    17
    1
    -

    Gastrointestinal motility disorder
    10
    <1
    - 
    7
    <1
    -

    Oral discomfort
    10
    -
    -
    10
    -
    -

    Skin and Subcutaneous Tissue

    Palmar-plantar erythrodysesthesia syndrome
    54
    17
    NA
    6
    1
    NA

    Dermatitis
    27
    1
    -
    26
    1
    -

    Hepatobiliary

    Hyperbilirubinemia
    48
    18
    5
    17
    3
    3

    General

    Fatigue*
    42
    4
    -
    46
    4
    -

    Pyrexia
    18
    1
    -
    21
    2
    -

    Edema
    15
    1
    -
    9
    1
    -

    Pain
    12
    1
    -
    10
    1
    -

    Metabolism and Nutrition

    Decreased appetite
    26
    3
    <1
    31
    2
    <1

    Respiratory Thoracic and Mediastinal

    Dyspnea
    14
    1
    -
    10
    <1
    1

    Eye

    Eye irritation
    13
    -
    -
    10
    <1
    -

    Nervous System

    Peripheral sensory neuropathy
    10
    -
    -
    4
    -
    -

    Headache
    10
    1
    -
    7
    -
    -

    Musculoskeletal

    Back pain
    10
    2
    -
    9
    <1
    -

    – Not observed

    * Includes weakness

    NA = Not Applicable

    Clinically relevant adverse reactions in <10% of patients are presented below:

    Eye:abnormal vision

    Gastrointestinal:upper gastrointestinal tract inflammatory disorders, gastrointestinal hemorrhage, ileus

    General:chest pain

    Infections:viral

    Metabolism and Nutrition:dehydration

    Musculoskeletal:arthralgia

    Nervous System:dizziness (excluding vertigo), insomnia, taste disturbance

    Psychiatric:mood alteration, depression

    Respiratory, Thoracic, and Mediastinal:cough, pharyngeal disorder

    Skin and Subcutaneous Tissue:skin discoloration, alopecia

    Vascular:venous thrombosis
    In Combination with Oxaliplatin

    The safety of capecitabine for the treatment of patients with unresectable or metastatic colorectal cancer as a component of a combination chemotherapy regimen was derived from published literature [see Clinical Studies (14.1)] . The safety of capecitabine for the treatment of patients with unresectable or metastatic colorectal cancer as a component of a combination chemotherapy regimen was similar to those in patients treated with capecitabine as a single agent, with the exception of an increased incidence of peripheral neuropathy.
    Metastatic Breast Cancer

    In Combination with Docetaxel

    The safety of capecitabine in combination with docetaxel was evaluated in patients with metastatic breast cancer in Study SO14999 [see Clinical Studies (14.2)] . Patients received capecitabine 1,250 mg/m 2orally twice daily for the first 14 days of a 21-day cycle with docetaxel 75 mg/m 2as 1- hour intravenous infusion on day 1 of each 21-day cycle for at least 6 weeks or docetaxel 100 mg/m 2as a 1-hour intravenous infusion on day 1 of each 21-day cycle for at least 6 weeks. Among patients who received capecitabine, the mean duration of treatment was 4.2 months.
    Permanent discontinuation due to an adverse reaction occurred in 26% of patients who received capecitabine. Dosage interruptions due to an adverse reaction occurred in 79% of patients who received capecitabine and dosage reductions due to an adverse reaction occurred in 65%.
    Most common adverse reactions (>30%) were diarrhea, stomatitis, palmar-plantar erythrodysesthesia syndrome, nausea, alopecia, vomiting, edema, and abdominal pain.
    Table 5 summarizes the adverse reactions in Study SO14999.

    Table 5 Adverse Reactions (≥10%) in Patients Who Received Capecitabine with Docetaxel for Metastatic Breast Cancer in Study SO14999


    Adverse Reaction
    Capecitabine with Docetaxel (N=251)
    Docetaxel (N=255)

    All
    Grades
    (%)
    Grade
    3 (%)
    Grade
    4 (%)
    All
    Grades
    (%)
    Grade
    3 (%)
    Grade
    4 (%)

    Gastrointestinal

    Diarrhea
    67
    14
    <1
    48
    5
    <1

    Stomatitis
    67
    17
    <1
    43
    5
    -

    Nausea
    45
    7
    -
    36
    2
    -

    Vomiting
    35
    4
    1
    24
    2
    -

    Abdominal pain
    30
    3
    <1
    24
    2
    -

    Constipation
    20
    2
    -
    18
    -
    -

    Dyspepsia
    14
    -
    -
    8
    1
    -

    Skin and Subcutaneous Tissue

    Palmar-plantar erythrodysesthesia

    syndrome
    63
    24
    NA
    8
    1
    NA

    Alopecia
    41
    6
    -
    42
    7
    -

    Nail disorder
    14
    2
    -
    15
    -
    -

    Cardiac

    Edema
    33
    <2
    -
    34
    <3
    1

    General

    Pyrexia
    28
    2
    -
    34
    2
    -

    Asthenia
    26
    4
    <1
    25
    6
    -

    Fatigue
    22
    4
    -
    27
    6
    -

    Weakness
    16
    2
    -
    11
    2
    -

    Pain in Limb
    13
    <1
    -
    13
    2
    -

    Blood and Lymphatic System

    Neutropenic fever
    16
    3
    13
    21
    5
    16

    Nervous System

    Taste disturbance
    16
    <1
    -
    14
    <1
    -

    Headache
    15
    3
    -
    15
    2
    -

    Paresthesia
    12
    <1
    -
    16
    1
    -

    Dizziness
    12
    -
    -
    8
    <1
    -

    Musculoskeletal and Connective Tissue

    Arthralgia
    15
    2
    -
    24
    3
    -

    Myalgia
    15
    2
    -
    25
    2
    -

    Back Pain
    12
    <1
    -
    11
    3
    -

    Respiratory, Thoracic and Mediastinal

    Dyspnea
    14
    2
    <1
    16
    2
    -

    Cough
    13
    1
    -
    22
    <1
    -

    Sore Throat
    12
    2
    -
    11
    <1
    -

    Metabolism and Nutrition

    Anorexia
    13
    <1
    -
    11
    <1
    -

    Appetite decreased
    10
    -
    -
    5
    -
    -

    Dehydration
    10
    2
    -
    7
    <1
    <1

    Eye

    Lacrimation increased
    12
    -
    -
    7
    <1
    -

    – Not observed

    NA = Not Applicable.
    Clinically relevant adverse reactions in <10% of patients are presented below:

    Blood and Lymphatic System:agranulocytosis, prothrombin decreased

    Cardiac:supraventricular tachycardia

    Eye:conjunctivitis, eye irritation

    Gastrointestinal:ileus, necrotizing enterocolitis, esophageal ulcer, hemorrhagic diarrhea, dry mouth

    General:chest pain (non-cardiac), lethargy, pain, influenza-like illness

    Hepatobiliary:jaundice, abnormal liver function tests, hepatic failure, hepatic coma, hepatotoxicity

    Immune System:hypersensitivity

    Infection:hypoesthesia, neutropenic sepsis, sepsis, bronchopneumonia, oral candidiasis, urinary tract infection

    Metabolism and Nutrition:weight decreased

    Musculoskeletal and Connective Tissue:bone pain

    Nervous System:insomnia, peripheral neuropathy, ataxia, syncope, taste loss, polyneuropathy, migraine

    Psychiatric:depression

    Renal and Urinary:renal failure

    Respiratory, Thoracic and Mediastinal:upper respiratory tract infection, pleural effusion, epistaxis, rhinorrhea

    Skin and Subcutaneous Tissue:pruritis, rash erythematous, dermatitis, nail discoloration, onycholysis

    Vascular:lymphedema, hypotension, venous phlebitis and thrombophlebitis, postural hypotension, flushing

    Table 6 summarizes the laboratory abnormalities in this trial.

    Table 6 Laboratory Abnormalities (≥20%) in Patients Who Received Capecitabine with Docetaxel for
    Metastatic Breast Cancer in Study SO14999


    Laboratory Abnormality
    Capecitabine with Docetaxel (N=251)
    Docetaxel (N=255)

    All
    Grades
    (%)
    Grade
    3 (%)
    Grade
    4 (%)
    All Grades
    (%)
    Grade
    3 (%)
    Grade
    4 (%)

    Hematologic

    Lymphocytopenia
    99
    48
    41
    98
    44
    40

    Leukopenia
    91
    37
    24
    88
    42
    33

    Neutropenia
    86
    20
    49
    87
    10
    66

    Anemia
    80
    7
    3
    83
    5
    <1

    Thrombocytopenia
    41
    2
    1
    23
    1
    2

    Hepatobiliary

    Hyperbilirubinemia
    20
    7
    2
    6
    2
    2

    Single Agent

    The safety of capecitabine as a single agent was evaluated in patients with metastatic breast cancer in Study SO14697 [see Clinical Studies (14.2)] . Patients received capecitabine 1,250 mg/m 2orally twice daily for the first 14 days of a 21-day cycle. The mean duration of treatment was 3.7 months.

    Permanent discontinuation due to an adverse reaction or intercurrent illness occurred in 8% of patients.

    Most common adverse reactions (>30%) were lymphopenia, anemia, diarrhea, hand-and-foot syndrome, nausea, fatigue, vomiting, and dermatitis.

    Table 7 summarizes the adverse reactions in Study SO14697.


    Table 7 Adverse Reactions (>10%) in Patients Who Received Capecitabine for Metastatic Breast Cancer
    in Study SO14697


    Adverse Reaction
    Capecitabine (n=162)

    All Grades (%)
    Grade 3 (%)
    Grade 4 (%)

    Blood and Lymphatic System

    Lymphopenia
    94
    44
    15

    Anemia
    72
    3
    1

    Neutropenia
    26
    2
    2

    Thrombocytopenia
    24
    3
    1

    Gastrointestinal

    Diarrhea
    57
    12
    3

    Nausea
    53
    4
    -

    Vomiting
    37
    4
    -

    Stomatitis
    24
    7
    -

    Abdominal pain
    20
    4
    -

    Constipation
    15
    1
    -

    Skin and Subcutaneous Tissue

    Hand-and-foot syndrome
    57
    11
    NA

    Dermatitis
    37
    1
    -

    General

    Fatigue
    41
    8
    -

    Pyrexia
    12
    1
    -

    Metabolism and Nutrition

    Anorexia
    23
    3
    -

    Hepatobiliary

    Hyperbilirubinemia
    22
    9
    2

    Nervous System

    Paresthesia
    21
    1
    -

    Eye

    Eye irritation
    15
    -
    -

    – = Not observed

    NA = Not Applicable  Pooled Safety Population

    Clinically relevant adverse reactions in <10% of patients who received capecitabine as a single agent are presented below.
    Blood & Lymphatic System:leukopenia, coagulation disorder, bone marrow depression, pancytopenia
    Cardiac:tachycardia, bradycardia, atrial fibrillation, myocarditis, edema
    Ear:vertigo
    Eye:conjunctivitis
    Gastrointestinal:abdominal distension, dysphagia, proctalgia, gastric ulcer, ileus, gastroenteritis, dyspepsia
    General:chest pain, influenza-like illness, hot flushes, pain, thirst, fibrosis, hemorrhage, edema, pain in limb
    Hepatobiliary:hepatic fibrosis, hepatitis, cholestatic hepatitis, abnormal liver function tests
    Immune System:drug hypersensitivity
    Infections:bronchitis, pneumonia, keratoconjunctivitis, sepsis, fungal infections
    Metabolism and Nutrition:cachexia, hypertriglyceridemia, hypokalemia, hypomagnesemia, dehydration
    Musculoskeletal and Connective Tissue:myalgia, arthritis, muscle weakness
    Nervous System:insomnia, ataxia, tremor, dysphasia, encephalopathy, dysarthria, impaired balance, headache, dizziness
    Psychiatric:depression, confusion
    Renal and Urinary:renal impairment
    Respiratory, Mediastinal and Thoracic:cough, epistaxis, respiratory distress, dyspnea
    Skin and Subcutaneous Tissue:nail disorder, sweating increased, photosensitivity reaction, skin ulceration, pruritus, radiation recall syndrome

    Vascular:hypotension, hypertension, lymphedema, pulmonary embolism


    Unresectable or Metastatic Gastric, Esophageal, or Gastroesophageal Junction CancerThe safety of capecitabine for the treatment of adults with unresectable or metastatic gastric, esophageal, or gastroesophageal junction cancer as a component of a combination chemotherapy regimen was derived from published literature [see Clinical Studies (14.3)]. The safety of capecitabine for the treatment of adults with unresectable or metastatic gastric, esophageal, or gastroesophageal junction cancer as a component of a combination chemotherapy regimen was consistent with the known safety profile of capecitabine.

    The safety of capecitabine for the treatment of patients with HER2-overexpressing metastatic gastric or gastroesophageal junction adenocarcinoma who have not received prior treatment for metastatic disease as a component of a combination regimen was derived from the published literature [see Clinical Studies (14.3)]. The safety of capecitabine for the treatment of patients with HER2-overexpressing metastatic gastric or gastroesophageal junction adenocarcinoma was consistent with the known safety profile of capecitabine.

    Pancreatic Cancer

    The safety of capecitabine for the adjuvant treatment of adults with pancreatic adenocarcinoma as a component of a combination chemotherapy regimen was derived from the published literature [ see Clinical Studies (14.4)]. The safety of capecitabine for the adjuvant treatment of adults with pancreatic adenocarcinoma as a component of a combination chemotherapy regimen was consistent with the known safety profile of capecitabine

    6.2 Postmarketing Experience

    The following adverse reactions have been identified during post-approval use of capecitabine. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

    Eye:lacrimal duct stenosis, corneal disorders including keratitis

    Hepatobiliary:hepatic failure

    Immune System Disorders:angioedema

    Nervous System:toxic leukoencephalopathy

    Renal & Urinary:acute renal failure secondary to dehydration including fatal outcome

    Skin & Subcutaneous Tissue:cutaneous lupus erythematosus, severe skin reactions such as Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis (TEN), persistent or severe PPES can eventually lead to loss of fingerprints

  • 7 DRUG INTERACTIONS

    7.1 Effect of Other Drugs on Capecitabine

    Allopurinol

    Concomitant use with allopurinol may decrease concentration of capecitabine’s active metabolites [see Clinical Pharmacology (12.3)] , which may decrease efficacy. Avoid concomitant use of allopurinol with capecitabine.
    Leucovorin

    The concentration of fluorouracil is increased and its toxicity may be enhanced by leucovorin, folic acid, or folate analog products. Deaths from severe enterocolitis, diarrhea, and dehydration have been reported in elderly patients receiving weekly leucovorin and fluorouracil.
    Instruct patients not to take products containing folic acid or folate analog products unless directed to do so by their healthcare provider.

    7.2 Effect of Capecitabine on Other Drugs

    CYP2C9 Substrates

    Capecitabine increased exposure of CYP2C9 substrates [ see Clinical Pharmacology (12.3)], which may increase the risk of adverse reactions related to these substrates. Closely monitor for adverse reactions of CYP2C9 substrates where minimal concentration changes may lead to serious adverse reactions when used concomitantly with capecitabine (e.g., anticoagulants, antidiabetic drugs).
    Vitamin K Antagonists

    Capecitabine increases exposure of vitamin K antagonist [ see Clinical Pharmacology (12.3)], which may alter coagulation parameters and/or bleeding and could result in death [ see Warning and Precautions (5.1)]. These events may occur within days of treatment initiation and up to 1 month after discontinuation of capecitabine.
    Monitor INR more frequently and refer to the prescribing information of oral vitamin K antagonist for dosage adjustment, as appropriate, when capecitabine is used concomitantly with vitamin K antagonist.
    Phenytoin

    Capecitabine may increases exposure of phenytoin, which may increase the risk of adverse reactions related to phenytoin. Closely monitor phenytoin levels and refer to the prescribing information of phenytoin for dosage adjustment, as appropriate, when capecitabine is used concomitantly with phenytoin.

    7.3 Nephrotoxic Drugs

    Due of the additive pharmacologic effect, concomitant use of capecitabine with other drugs known to cause renal toxicity may increase the risk of renal toxicity [ see Warnings and Precautions (5.6)]. Closely monitor for signs of renal toxicity when capecitabine is used concomitantly with nephrotoxic drugs (e.g. platinum salts, irinotecan, methotrexate, intravenous bisphosphonates).

  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Risk Summary

    Based on findings in animal reproduction studies and its mechanism of action [see Clinical Pharmacology (12.1)] , capecitabine can cause fetal harm when administered to a pregnant woman. Available human data with capecitabine use in pregnant women is not sufficient to inform the drug-associated risk. In animal reproduction studies, administration of capecitabine to pregnant animals during the period of organogenesis caused embryolethality and teratogenicity in mice and embryolethality in monkeys at 0.2 and 0.6 times the exposure (AUC) in patients receiving the recommended dose of 1,250 mg/m 2 twice daily, respectively (see Data). Advise pregnant women of the potential risk to a fetus. 

    The estimated background risk of major birth defects and miscarriage for the indicated population is unknown. All pregnancies have a background risk of birth defect, loss, or other adverse outcomes. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively.
    Data

    Animal Data

    Oral administration of capecitabine to pregnant mice during the period of organogenesis at a dose of 198 mg/kg/day caused malformations and embryo lethality. In separate pharmacokinetic studies, this dose in mice produced 5’-DFUR AUC values that were approximately 0.2 times the AUC values in patients administered the recommended daily dose. Malformations in mice included cleft palate, anophthalmia, microphthalmia, oligodactyly, polydactyly, syndactyly, kinky tail and dilation of cerebral ventricles. Oral administration of capecitabine to pregnant monkeys during the period of organogenesis at a dose of 90 mg/kg/day, caused fetal lethality. This dose produced 5’-DFUR AUC values that were approximately 0.6 times the AUC values in patients administered the recommended daily dose.

    8.2 Lactation

    Risk Summary

    There is no information regarding the presence of capecitabine or its metabolites in human milk, or on its effects on milk production or the breastfed child. Capecitabine metabolites were present in the milk of lactating mice (see Data). Because of the potential for serious adverse reactions in a breastfed child, advise women not to breastfeed during treatment with capecitabine and for 1 week after the last dose.

    Data

    Lactating mice given a single oral dose of capecitabine excreted significant amounts of capecitabine metabolites into the milk.

    8.3 Females and Males of Reproductive Potential

    Capecitabine can cause fetal harm when administered to a pregnant woman [see Use in Specific Populations (8.1)] .

    Pregnancy Testing

    Verify pregnancy status in females of reproductive potential prior to initiating capecitabine.

    Contraception

    Females

    Advise females of reproductive potential to use effective contraception during treatment with capecitabine and for 6 months after the last dose.

    Males

    Based on genotoxicity findings, advise males with female partners of reproductive potential to use effective contraception during treatment with capecitabine and for 3 months after the last dose [see Nonclinical Toxicology (13.1)] .

    Infertility

    Based on animal studies, capecitabine may impair fertility in females and males of reproductive potential [see Nonclinical Toxicology (13.1)] .

    8.4 Pediatric Use

    The safety and effectiveness of capecitabine in pediatric patients have not been established.
    Safety and effectiveness were assessed, but not established in two single arm studies in 56 pediatric patients aged 3 months to <17 years with newly diagnosed gliomas. In both trials, pediatric patients received an investigational pediatric formulation of capecitabine concomitantly with and following completion of radiation therapy (total dose of 5580 cGy in 180 cGy fractions). The relative bioavailability of the investigational formulation to capecitabine was similar.
    The adverse reaction profile was consistent with that of adults, with the exception of laboratory abnormalities which occurred more commonly in pediatric patients. The most frequently reported laboratory abnormalities (per-patient incidence ≥ 40%) were increased ALT (75%), lymphocytopenia (73%), hypokalemia (68%), thrombocytopenia (57%), hypoalbuminemia (55%), neutropenia (50%), low hematocrit (50%), hypocalcemia (48%), hypophosphatemia (45%) and hyponatremia (45%).

    8.5 Geriatric Use

    Of 7938 patients with colorectal cancer who were treated with capecitabine, 33% were older than 65 years. Of the 4536 patients with metastatic breast cancer who were treated with capecitabine, 18% were older than 65 years.

    Of 1951 patients with gastric, esophageal, or gastrointestinal junction cancer who were treated with capecitabine, 26% were older than 65 years.

    Of 364 patients with pancreatic cancer who received adjuvant treatment with capecitabine, 47% were 65 years or older.

    No overall differences in efficacy were observed comparing older versus younger patients with colorectal cancer, gastric, esophageal or gastrointestinal junction cancer, or pancreatic cancer using the approved recommended dosages and treatment regimens.

    Older patients experience increased gastrointestinal toxicity due to capecitabine compared to younger patients. Deaths from severe enterocolitis, diarrhea, and dehydration have been reported in elderly patients receiving weekly leucovorin and fluorouracil [see Drug Interactions (7.1)].

    8.6 Renal Impairment

    The exposure of capecitabine and its inactive metabolites (5-DFUR and FBAL) increases in patients with CLcr <50 mL/min as determined by Cockcroft-Gault [see Clinical Pharmacology (12.3)]. Reduce the dosage for patients with CLcr of 30 to 50 mL/min [ see Dosage and Administration (2.6)]. There is limited experience with capecitabine in patients with CLcr <30 mL/min, and a dosage has not been established in those patients. If no treatment alternative exists, capecitabine could be administered to such patients on an individual basis applying a reduced starting dose, close monitoring of a patient's clinical and biochemical data and dose modifications guided by observed adverse reactions.

    8.7 Hepatic Impairment

    The exposure of capecitabine increases in patients with mild to moderate hepatic impairment.
    The effect of severe hepatic impairment on the safety and pharmacokinetics of capecitabine is unknown [ see Clinical Pharmacology (12.3)] .Monitor patients with hepatic impairment more frequently for adverse reactions.

  • 10 OVERDOSAGE

    Administer uridine triacetate within 96 hours for management of capecitabine overdose.
    Although no clinical experience using dialysis as a treatment for capecitabine overdose has been reported, dialysis may be of benefit in reducing circulating concentrations of 5’-DFUR, a low–molecular-weight metabolite of the parent compound. 

  • 11 DESCRIPTION

    Capecitabine is a nucleoside metabolic inhibitor. The chemical name is 5’-deoxy-5-fluoro-N- [(pentyloxy) carbonyl]-cytidine and has a molecular formula of C 15H 22FN 3O 6and a molecular weight of 359.35. Capecitabine has the following structural formula:


    Cape

    Capecitabine is a white to off-white crystalline powder with an aqueous solubility of 26 mg/mL at 20ºC.

    Capecitabine Tablets, USP are supplied as biconvex, oblong film-coated tablets for oral use. Each light peach- colored tablet debossed with ‘C150’ on one side and plain on other side contains 150 mg of capecitabine USP and each peach colored tablet debossed with ‘C500’ on one side and plain on other side contains 500 mg of capecitabine USP. The inactive ingredients in capecitabine include: anhydrous lactose, croscarmellose sodium, hydroxypropyl methylcellulose, microcrystalline cellulose, magnesium stearate. The peach or light peach film coating contains hydroxypropyl methylcellulose, polyethylene glycol, red iron oxides, synthetic yellow, talc and titanium dioxide.

  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    Capecitabine is metabolized to fluorouracil in vivo. Both normal and tumor cells metabolize fluorouracil to 5-fluoro-2’-deoxyuridine monophosphate (FdUMP) and 5-fluorouridine triphosphate (FUTP). These metabolites cause cell injury by two different mechanisms. First, FdUMP and the folate cofactor, N 5-10-methylenetetrahydrofolate, bind to thymidylate synthase (TS) to form a covalently bound ternary complex. This binding inhibits the formation of thymidylate from 2’-deoxyuridylate. Thymidylate is the necessary precursor of thymidine triphosphate, which is essential for the synthesis of DNA, so that a deficiency of this compound can inhibit cell division. Second, nuclear transcriptional enzymes can mistakenly incorporate FUTP in place of uridine triphosphate (UTP) during the synthesis of RNA. This metabolic error can interfere with RNA processing and protein synthesis.

    12.2 Pharmacodynamics

    Population-based exposure-effect analyses demonstrated a positive association between AUC of fluorouracil and grade 3-4 hyperbilirubinemia.

    12.3 Pharmacokinetics

    The AUC of capecitabine and its metabolite 5’-DFCR increases proportionally over a dosage range of 500 mg/m 2/day to 3,500 mg/m 2/day (0.2 to 1.4 times the approved recommended dosage).The AUC of capecitabine’s metabolites 5’-DFUR and fluorouracil increased greater than proportional to the dose. The interpatient variability in the C maxand AUC of fluorouracil was greater than 85%.
    AbsorptionFollowing oral administration of capecitabine 1,255 mg/m 2orally twice daily (the recommended dosage when used as single agent), the median T max of capecitabine and its metabolite fluorouracil was approximately 1.5 hours and 2 hours, respectively.

    Effect of Food

    Following administration of a meal (breakfast medium-rich in fat and carbohydrates), the mean C maxand AUC 0-INFof capecitabine was decreased by 60% and 34%, respectively. The mean C maxand AUC 0-INFof fluorouracil were also decreased by 37% and 12%, respectively. The T maxof both capecitabine and fluorouracil was delayed by1.5 hours.
    Distribution

    Plasma protein binding of capecitabine and its metabolites is less than 60% and is not concentration-dependent.Capecitabine was primarily bound to human albumin (approximately 35%).
    Following oral administration of capecitabine 7 days before surgery in patients with colorectal cancer, the median ratio of concentration for the active metabolite fluorouracil in colorectal tumors to adjacent tissues was 2.9 (range: 0.9 to 8.0).
    Elimination
    The elimination half-lives of capecitabine and fluorouracil were approximately0.75 hour.
    Metabolism
    Capecitabine undergoes metabolism by carboxylesterase and is hydrolyzed to 5’-DFCR. 5’- DFCR is subsequently converted to 5’-DFUR by cytidine deaminase. 5’-DFUR is then hydrolized by thymidine phosphorylase (dThdPase) enzymes to the active metabolite fluorouracil.
    Fluorouracil is subsequently metabolized by dihydropyrimidine dehydrogenase to 5-fluoro-5,6- dihydro-fluorouracil (FUH 2). The pyrimidine ring of FUH 2is cleaved by dihydropyrimidinase to yield 5-fluoro-ureido-propionic acid (FUPA). Finally, FUPA is cleaved by β-ureido-propionase to α-fluoro-β-alanine (FBAL).
    Excretion
    Following administration of radiolabeled capecitabine,96% of the administered capecitabine dose was recovered in urine (3% unchanged and 57% as metabolite FBAL) and 2.6% in feces.
    Specific Populations
    Following therapeutic doses of capecitabine, no clinically meaningful difference in the pharmacokinetics of 5’-DFUR, fluorouracil or FBAL were observed based on sex (202 females and 303 males) and race (455 White, 22 Black, and 28 Other). No clinically meaningful difference on the pharmacokinetics of 5’-DFUR and fluorouracil were observed based on age (range: 27 to 86 years); however, the AUC of FBAL increased by 15% following a 20% increase in age.
    Racial or Ethnic Groups

    Following administration of capecitabine 825 mg/m 2orally twice daily for 14 days (0.66 times the recommended dosage), the C maxand AUC of capecitabine decreased by 36% and 24%, respectively in Japanese patients (n=18) compared to White patients (n=22). The C maxand AUC of FBAL decreased by approximately 25% and 34%, respectively in Japanese patients compared to White patients; however, the clinical significance of these differences is unknown. No clinically significant differences in the pharmacokinetics of 5’-DFCR, 5’-DFUR or fluorouracil were observed.

    Patients with Renal Impairment
    Table 8 Effect of Renal Impairment on the Pharmacokinetics of Capecitabine, 5’-DFUR, and FBAL

    Renal
    Impairment a    		Changes in AUC b
    Capecitabine5’-DFUR cFBAL c5-FU
    Lcr 30 to 50
    mL/min     		Increased by 25%Increased by 42%Increased by 85%No relevant
    change
    CLcr <30 mL/minIncreased by 25%Increased by 71%Increased by
    258%     		Increased by 24%
    aCompared to patients with CLcr >80 mL/min
    bFollowing administration of capecitabine 1,250 mg/ m 2orally twice daily; day 1 observations
    cCapecitabine metabolite
    CLcr=Creatine Clearance, AUC= Area under the plasma concentration-time curve

    Patients with Hepatic Impairment

    AUC 0-INFand C maxof capecitabine’s active principle, fluorouracil, were not affected in patients with mild or moderate hepatic impairment compared to patients with normal hepatic function. The AUC 0-INFand C maxof capecitabine increased by 60%. The effect of severe hepatic impairment on the pharmacokinetics of capecitabine and its metabolites are unknown.

    Drug Interaction Studies

    Clinical Studies
    Effect of Capecitabine on Warfarin: In four patients with cancer, chronic administration of capecitabine 1,250 mg/m 2twice daily with a single dose of warfarin 20 mg increased the mean AUC of S-warfarin by 57% and decreased its clearance by 37%. Baseline corrected AUC of INR in these 4 patients increased by 2.8-fold, and the maximum observed mean INR value was increased by 91%.
    Effect of Capecitabine on Celecoxib: Concomitant administration of multiple doses of capecitabine (capecitabine 1,000 mg/m 2twice daily for 14 days) increased celecoxib (sensitive CYP2C9 substrate) AUC by 28%, C max by 24% and C troughby 30%.
    Effect of Antacids on Capecitabine: When an aluminum hydroxide- and magnesium hydroxide containing antacid was administered immediately after a capecitabine dose of 1,250 mg/m 2 in patients with cancer, AUC and C max increased by 16% and 35%, respectively, for capecitabine and by 18% and 22%, respectively, for 5’-DFCR. No effect was observed on the other three major metabolites (5’-DFUR, fluorouracil, FBAL) of capecitabine
    Effect of Allopurinol on Capecitabine: Concomitant use with allopurinol may decrease conversion of capecitabine to the active metabolites, FdUMP and FUTP.
    Effect of Capecitabine on Docetaxel and Effect of Docetaxel on Capecitabine: Capecitabine had no effect on the pharmacokinetics of docetaxel (C max and AUC) and docetaxel has no effect on the pharmacokinetics of capecitabine and the fluorouracil precursor 5’-DFUR.
    In Vitro Studies
    Cytochrome P450 (CYP) Enzymes: Capecitabine and its metabolites (5’-DFUR, 5’-DFCR, fluorouracil, and FBAL) did not inhibit CYP1A2, CYP2A6, CYP3A4, CYP2C19, CYP2D6, or CYP2E1 in vitro.

    12.5 Pharmacogenomics

    The DPYDgene encodes the enzyme DPD, which is responsible for the catabolism of >80% of fluorouracil. Approximately 3-5% of White populations have partial DPD deficiency and 0.2% of White populations have complete DPD deficiency, which may be due to certain genetic no function or decreased function variants in DPYDresulting in partial to complete or near complete absence of enzyme activity. DPD deficiency is estimated to be more prevalent in Black or African American populations compared to White populations. Insufficient information is available to estimate the prevalence of DPD deficiency in other populations.

    Patients who are homozygous or compound heterozygous for no function DPYDvariants (i.e., carry two no function DPYDvariants) or are compound heterozygous for a no function DPYDvariant plus a decreased function DPYDvariant have complete DPD deficiency and are at increased risk for acute early-onset of toxicity and serious life-threatening, or fatal adverse reactions due to increased systemic exposure to capecitabine. Partial DPD deficiency can result from the presence of either two decreased function DPYDvariants or one normal function plus either a decreased function or a no function DPYDvariant. Patients with partial DPD deficiency may also be at an increased risk for toxicity from capecitabine.
    Four DPYDvariants have been associated with impaired DPD activity in White populations, especially when present as homozygous or compound heterozygous variants: c.1905+1G>A ( DPYD*2A), c.1679T>G ( DPYD*13), c.2846A>T, and c.1129-5923C>G (Haplotype B3). DPYD*2A and DPYD*13 are no function variants, and c.2846A>T and c.1129-5923C >G are decreased function variants. The decreased function DPYDvariant c.557A>G is observed in individuals of African ancestry. This is not a complete listing of all DPYD variants that may result in DPD deficiency [ see Warnings and Precautions (5.2)].

  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    Adequate studies investigating the carcinogenic potential of capecitabine have not been conducted. Capecitabine was not mutagenic in vitro to bacteria (Ames test) or mammalian cells (Chinese hamster V79/HPRT gene mutation assay). Capecitabine was clastogenic in vitroto human peripheral blood lymphocytes but not clastogenic in vivoto mouse bone marrow (micronucleus test). Fluorouracil causes mutations in bacteria and yeast. Fluorouracil also causes chromosomal abnormalities in the mouse micronucleus test in vivo. 

    In studies of fertility and general reproductive performance in female mice, oral capecitabine doses of 760 mg/kg/day (about 2300 mg/m 2/day) disturbed estrus and consequently caused a decrease in fertility. In mice that became pregnant, no fetuses survived this dose. The disturbance in estrus was reversible. In males, this dose caused degenerative changes in the testes, including decreases in the number of spermatocytes and spermatids. In separate pharmacokinetic studies, this dose in mice produced 5’-DFUR AUC values about 0.7 times the corresponding values in patients administered the recommended daily dose. 

  • 14 CLINICAL STUDIES

    14.1 Colorectal Cancer

    Adjuvant Treatment of Colon Cancer

    Single Agent
    The efficacy of capecitabine was evaluated in X-ACT( NCT00009737), a multicenter, randomized, controlled clinical trial. Eligible patients were between 18 and 75 years of age with histologically-confirmed Dukes’ Stage C colon cancer with at least one positive lymph node and to have undergone (within 8 weeks prior to randomization) complete resection of the primary tumor without macroscopic or microscopic evidence of remaining tumor. Patients were also required to have no prior cytotoxic chemotherapy or immunotherapy (except steroids) and have an ECOG performance status of 0 or 1 (KPS ≥70%), ANC ≥1.5x10 9/L,platelets ≥100x10 9/L,serum creatinine ≤1.5ULN, total bilirubin ≤1.5 ULN,AST/ALT≤2.5 ULN and CEA within normal limits at time of randomization.
    Patients (n=1987) were randomized to capecitabine1,250 mg/m 2orally twice daily for the first 14 days of a 21-day cycle for a total of 8 cycles or fluorouracil 425 mg/m 2and leucovorin 20 mg/m 2intravenously on days 1 to 5 of each 28-day cycle for a total of 6 cycles. The capecitabine dose was reduced in patients with baseline CLcr of 30 to 50 mL/min. The major efficacy outcome measure was disease-free survival (DFS).
    The baseline demographics are shown in Table 9.The baseline characteristics were well balanced between arms.



    Table 9 Baseline Demographics in X-ACT




    Capecitabine (N=1004)


    Fluorouracil+Leucovorin (N=983)

    Age (median, years)
    62
    63

    Range
    (25-80)
    (22-82)

    Sex

    Male,%
    54
    54

    Female,%
    46
    46

    ECOG Performance Status

    0,%
    85
    85

    1,%
    15
    15

    Staging–Primary Tumor

    PT1,%
    1
    0.6

    PT2,%
    9
    9

    PT3,%
    76
    76

    PT4,%
    14
    0

    Other,%
    0.1
    14

    Staging–Lymph Node

    pN1,%
    69
    71

    pN2, %
    30
    29

    Other,%
    0.4
    0.1

    Efficacy results are summarized in Table 10 and Figures 1 and 2. The median follow-up at the time of the analysis was 6.9 years. Because the upper 2-sided 95% confidence limit of hazard ratio for DFS was less than 1.20, capecitabine was non-inferior to fluorouracil + leucovorin. The choice of the non-inferiority margin of 1.20 corresponds to the retention of approximately 75% of the fluorouracil + leucovorin effect on DFS. The hazard ratio for capecitabine compared to fluorouracil + leucovorin with respect to overall survival was 0.86 (95% CI 0.74,1.01). The 5- year overall survival rates were 71% for capecitabine and 68% for fluorouracil + leucovorin.



    Table 10 Efficacy Results in X-ACT a(All Randomized Population)



    Efficacy Parameters

    Capecitabine
    (N=1004)



    Fluorouracil+Leucovorin(N=983)


    5-year Disease-free Survival Rate b
    59%
    55%

    Hazard Ratio
    0.88

    (95%CI)
    (0.77,1.01)

    p-value c
    p=0.068

    aApproximately 93.4% had 5-year DFS information
    bBased on Kaplan-Meier estimates
    cWald chi-square test

    Figure-1

    Figure-2


    In Combination with Oxaliplatin-Containing Regimens
    The efficacy of capecitabine in combination with oxaliplatin for the adjuvant treatment of patients with Stage III colon cancer as a component of a combination chemotherapy regimen was derived from studies in the published literature, including NO16968 [ NCT00069121], a multicenter, open-label, randomized trial, where the major efficacy outcome measure was disease free survival.
    Perioperative Treatment of Rectal Cancer
    The efficacy of capecitabine for the perioperative treatment of adults with locally advanced rectal cancer as a component of chemoradiotherapy was derived from studies in the published literature, including Rektum-III [ NCT01500993], a randomized, open-label, multicenter, non-inferiority trial, where the major efficacy outcome measure was overall survival.
    Metastatic Colorectal Cancer
    The efficacy of capecitabine as a single agent was evaluated in two open-label, multicenter, randomized, controlled clinical trials (Study SO14695 and Study SO14796). Eligible patients received first-line treatment for metastatic colorectal cancer. Patients were randomized to capecitabine 1,250 mg/m 2twice daily for first 14 days of a 21-day cycle or leucovorin 20 mg/m 2intravenously followed by fluorouracil 425 mg/m 2as an intravenous bolus on days 1 to 5 of each 28-day cycle.
    The efficacy outcome measures were overall survival, time to progression and response rate (complete plus partial responses). Responses were defined by the World Health Organization criteria and submitted to a blinded independent review committee (IRC). Differences in assessments between the investigator and IRC were reconciled by the sponsor, blinded to treatment arm, according to a specified algorithm. Survival was assessed based on a non-inferiority analysis. 
    The baseline demographics are shown in Table 11.


    Table 11 Baseline Demographics for Study SO14695 and Study SO14796




    Study SO14695

    Study SO14796


    Capecitabine (N=302)

    Fluorouracil + Leucovorin (N=303)

    Capecitabine (N=301)

    Fluorouracil + Leucovorin (N=301)

    Age (median, years)
    64
    63
    64
    64

    Range
    (23-86)
    (24-87)
    (29-84)
    (36-86)

    Sex

    Male, %
    60
    65
    57
    57

    Female, %
    40
    35
    43
    43

    Karnofsky PS (median)
    90
    90
    90
    90

    Range
    (70-100)
    (70-100)
    (70-100)
    (70-100)

    Colon,%
    74
    77
    66
    65

    Rectum,%
    26
    23
    34
    35

    Prior radiation therapy,%
    17
    21
    14
    14

    Prioradjuvant fluorouracil,%
    28
    36
    19
    14




    Efficacy results for Study SO14695 and Study SO14796 are shown in Table 12 and Table 13.

    Table 12 Efficacy Results for First-Line Treatment of Metastatic Colorectal Cancer (Study SO14695)



    Capecitabine (N=302)

    Fluorouracil +Leucovorin(N=303)


    Overall Response Rate

    %(95% CI)
    21(16, 26)
    11(8, 15)

    p-value
    0.0014


    Time to Progression

    Median, months(95%CI)
    4.2(3.9, 4.5)
    4.3(3.4, 5.0)

    Hazard Ratio
    0.99

    95% CI
    (0.84, 1.17)


    Overall Survival

    Median, months(95%CI)
    12.5(10.5, 14.3)
    13.4(12.0, 14.7)

    Hazard Ratio
    1.00

    95% CI
    (0.84, 1.18)


    Table 13 Efficacy Results for First-Line Treatment of Metastatic Colorectal Cancer (Study SO14796)




    Capecitabine(N=301)
    Fluorouracil+Leucovorin(N=301)


    Overall Response Rate

    %(95% CI)
    21(16, 26)
    14(10, 18)

    p-value
    0.027


    Time to Progression

    Median, months (95% CI)
    4.5 (4.2, 5.5)
    4.3 (3.4, 5.1)

    Hazard Ratio
    0.97

    95%CI
    (0.82,1.14)


    Overall Survival

    Median, months(95%CI)
    13.3 (12.1, 14.8)
    12.1 (11.1,14.1)

    Hazard Ratio
    0.92

    95% CI
    (0.78, 1.09)

    Efficacy results of the pooled population from Study SO14695 and Study SO14796 are shown in Figure 3. Statistical analyses were performed to determine the percent of the survival effect of fluorouracil +leucovorin that was retained by capecitabine. The estimate of the survival effect of fluorouracil + leucovorin was derived from a meta-analysis of ten randomized studies from the published literature comparing fluorouracil to regimens of fluorouracil + leucovorin that were similar to the control arms used in these Studies SO14695 and SO14796. The method for comparing the treatments was to examine the worst case (95% confidence upper bound) for the difference between fluorouracil + leucovorin and capecitabine, and to show that loss of more than 50% of the fluorouracil + leucovorin survival effect was ruled out. It was demonstrated that the percent of the survival effect of fluorouracil + leucovorin maintained was at least 61% for Study SO14796 and 10% for Study SO14695. The pooled result is consistent with a retention of at least 50% of the effect of fluorouracil + leucovorin. It should be noted that these values for preserved effect are based on the upper bound of the fluorouracil +leucovorin vs capecitabine difference.

    Figure-3

    In Combination with Oxaliplatin.

    The efficacy of capecitabine for the treatment of patients with unresectable or metastatic colorectal cancer as a component of a combination chemotherapy regimen was derived from studies in the published literature, including NO16966 [ NCT00069095], a randomized, non-inferiority, 2x2 factorial trial, where the major efficacy outcome measure was progression free survival.

    14.2 Metastatic Breast Cancer

    In Combination With Docetaxel

    The efficacy of capecitabine in combination with docetaxel was evaluated in an open-label, multicenter, randomized trial (Study SO14999). Eligible patients had metastatic breast cancer resistant to, or recurring during or after an anthracycline-containing therapy, or relapsing during or recurring within 2 years of completing an anthracycline-containing adjuvant therapy were enrolled. Patients were randomized to capecitabine 1,250 mg/m 2twice daily for the first 14 days of a 21-day cycle and docetaxel 75 mg/m2 as a 1-hour intravenous infusion on day 1 of day of a 21- day cycle or docetaxel 100 mg/m 2as a 1-hour intravenous infusion on day 1 of a 21-day cycle. The efficacy outcome measures were time to disease progression, overall survival, and response rate.

    Patient demographics are provided in Table 14.

    Table 14 Baseline Demographics in Metastatic Breast Cancer (Study SO14999)



    Capecitabine + Docetaxel (N=255)
    Docetaxel (N=256)

    Age (median, years)
    52
    51

    Karnofsky Performance Status (median)
    90
    90

    Site of Disease

    Lymph nodes, %
    47
    49

    Liver, %
    45
    48

    Bone, %
    42
    46

    Lung, %
    37
    39

    Skin, %
    29
    29

    Prior Chemotherapy

    Anthracycline 1, %
    100
    100

    Fluorouracil, %
    77
    74

    Paclitaxel, %
    10
    9

    Resistance to an Anthracycline

    No resistance, %
    7
    7

    Progression on anthracycline therapy, %
    26
    29

    Stable disease after 4 cycles of anthracycline therapy, %
    16
    16

    Relapsed within 2 years of completion of anthracycline-adjuvant therapy, %
    31
    29

    Experienced a brief response to anthracycline therapy, with subsequent progression while on therapy or within 12 months after last dose, %
    20
    20

    No. of Prior Chemotherapy Regimens for Treatment of Metastatic Disease

    0, %
    35
    31

    1, %
    48
    53

    2, %
    17
    15

    3, %
    0
    1

    1Includes 10 patients in combination and 18 patients in single agent arms treated with an anthracenedione

    Efficacy results are shown in Table 15, Figure 4 and Figure 5.


    Table 15 Efficacy Results in Metastatic Breast Cancer (Study SO14999)



    Efficacy Parameter

    Capecitabine + Docetaxel (N=255)

    Docetaxel
    (N=256)


    Time to Disease Progression

    Median, months
    6.1
    4.2

    95% CI
    (5.4, 6.5)
    (3.5, 4.5)

    Hazard Ratio
    0.643

    p-value
    0.0001


    Overall Survival

    Median, months
    14.5
    11.6

    95% CI
    (12.3, 16.3)
    (9.8, 12.7)

    Hazard Ratio
    0.775

    p-value
    0.0126


    Response Rate 1
    32%
    22%

    1The response rate reported represents a reconciliation of the investigator and IRC assessments performed by the sponsor according to a predefined algorithm.

    Figure-4

    Figure-5


    Single Agent
    The efficacy of capecitabine as a single agent was evaluated in an open-label single-arm trial (Study SO14697). Eligible patients had metastatic breast cancer resistant to both paclitaxel and an anthracycline-containing chemotherapy regimen or resistant to paclitaxel and for whom further anthracycline therapy is not indicated (e.g., patients who have received cumulative doses of 400 mg/m 2of doxorubicin or doxorubicin equivalents). Resistance was defined as progressive disease while on treatment, with or without an initial response, or relapse within 6 months of completing treatment with an anthracycline-containing adjuvant chemotherapy regimen. Patients received capecitabine 1,255 mg/m 2orally twice daily for first 14-days of a 21-day treatment cycle. The major efficacy outcome measure was tumor response rate in patients with measurable disease, with response defined as a ≥50% decrease in sum of the products of the perpendicular diameters of bidimensionally measurable disease for at least 1 month.
    The baseline demographics are shown in Table 16.

    Table 16 Baseline Demographics in Metastatic Breast Cancer (Study SO14697)



    Patients With Measurable Disease (N=135)

    All Patients (N=162)

    Age (median, years)
    55
    56

    Karnofsky Performance Status
    90
    90

    No. Disease Sites

    1-2, %
    32
    37

    3-4, %
    46
    43

    >5, %
    22
    21

    Dominant Site of Disease

    Visceral 1, %
    75
    68

    Soft Tissue, %
    22
    22

    Bone, %
    3
    10

    Prior Chemotherapy

    Paclitaxel, %
    100
    100

    Anthracycline 2, %
    90
    91

    Fluorouracil, %
    81
    82

    Resistance to Paclitaxel, %
    76
    77

    Resistance to an Anthracycline 2, %
    41
    41

    Resistance to both Paclitaxel and an Anthracycline 2, %
    32
    31

    1Lung, pleura, liver, peritoneum
    2Includes 2 patients treated with an anthracenedione

    Efficacy for Study SO14697 are shown in Table 17.

    Table 17 Efficacy Results in Metastatic Breast Cancer (Study SO14697)



    Efficacy Parameter

    Resistance to Both Paclitaxel and an
    Anthracycline (N=43)


    Response Rate 1
    (95% CI)
    25.6%
    (13.5, 41.2)

    Complete Response
    0%

    Partial Response 1
    11%


    Duration of Response 1
    Median, months 2
    (Range)

    5.1 (2.1-7.7) 

    1Includes 2 patients treated with an anthracenedione
    2From date of first response

    For the subgroup of 43 patients who were doubly resistant, the median time to progression was 3.4 months and the median survival was 8.4 months. The objective response rate in this population was supported by a response rate of 18.5% (1 CR, 24 PRs) in the overall population of 135 patients with measurable disease, who were less resistant to chemotherapy ( see Table 15). The median time to progression was 3.0 months and the median survival was 10.1 months.

    14.3 Gastric, Esophageal, or Gastroesophageal Junction Cancer

    The efficacy of capecitabine for treatment of adults with unresectable or metastatic gastric, esophageal, or gastroesophageal junction cancer as a component of a combination chemotherapy regimen was derived from studies in the published literature. capecitabine was evaluated in REAL-2, a randomized non-inferiority, 2x2 factorial trial, where the major efficacy outcome measure was overall survival, and  an additional randomized trial conducted by the North Central Cancer Treatment Group, where the major efficacy outcome measure was objective response rate.

    The efficacy of capecitabine for the treatment of adults with HER2-overexpressing metastatic gastric or gastroesophageal junction adenocarcinoma who have not received prior treatment for metastatic disease as a component of a combination regimen was derived from studies in the published literature. Capecitabine was evaluated in the ToGA trial [ NCT01041404], an open-label, multicenter, randomized trial where the primary efficacy measure was overall survival.

    14.4 Pancreatic Cancer

    The efficacy of capecitabine for the adjuvant treatment of adults with pancreatic adenocarcinoma as a component of a combination chemotherapy regimen was derived from a study in the published literature. Capecitabine was evaluated in ESPAC-4 trial, a two-group, open-label, multicenter, randomized trial, where the major efficacy outcome measure was overall survival.

  • 15 REFERENCES

    1. “OSHA Hazardous Drugs.” OSHA.  http://www.osha.gov/SLTC/hazardousdrugs/index.html.

  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    Capecitabine Tablets, USP are available as follows:

    150 mg

    Color:  Light peach

    Engraving: C150 on one side and plain on the other 

    150 mg tablets are packaged in bottles of 60 (NDC: 62135-783-60).  

    500 mg

    Color: Peach

    Engraving: C500 on one side and plain on the other 

    500 mg tablets are packaged in bottles of 120 (NDC: 62135-784-12).  

    Storage and Handling

    Store at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F). [See USP Controlled Room Temperature]. Keep tightly closed. 

    Capecitabine is a cytotoxic drug. Follow applicable special handling and disposal procedures 1.

  • 17 PATIENT COUNSELING INFORMATION

    Advise the patient to read the FDA-approved patient labeling ( Patient Information).

    Increased Risk of Bleeding with Concomitant Use of Vitamin K Antagonists

    Advise patients on vitamin K antagonists, such as warfarin, that they are at an increased risk of severe bleeding while taking capecitabine. Advise these patients that INR should be monitored more frequently, and dosage modifications of the vitamin K antagonist may be required, while taking and after discontinuation of capecitabine. Advise these patients to immediately contact their healthcare provider if signs or symptoms of bleeding occur [ see Warnings and Precautions (5.1)].

    Serious Adverse Reactions from Dihydropyrimidine Dehydrogenase (DPD) Deficiency

    Inform patients of the potential for serious and life-threatening adverse reactions due to DPD deficiency and discuss with your patient whether they should be tested for genetic variants of DPYD that are associated with an increased risk of serious adverse reactions from the use of capecitabine. Advise patients to immediately contact their healthcare provider if symptoms of severe mucositis, diarrhea, neutropenia, and neurotoxicity occur [ see Warnings and Precautions (5.2)and Clinical Pharmacology (12.5)].

    Cardiotoxicity

    Advise patients of the risk of cardiotoxicity and to immediately contact their healthcare provider for new onset of chest pain, shortness of breath, dizziness, or lightheadedness [ see Warnings and Precautions (5.3)].

    Diarrhea

    Inform patients experiencing grade 2 diarrhea (an increase of 4 to 6 stools/day or nocturnal stools) or greater or experiencing severe bloody diarrhea with severe abdominal pain and fever to stop taking capecitabine. Advise patients on the use of antidiarrheal treatments (e.g., loperamide) to manage diarrhea [see Warnings and Precautions (5.4)].

    Dehydration

    Instruct patients experiencing grade 2 or higher dehydration (IV fluids indicated < 24 hours) to stop taking capecitabine immediately and to contact their healthcare provider to correct the dehydration. Advise patients to not restart capecitabine until rehydrated and any precipitating causes have been corrected or controlled [see   Warnings and Precautions (5.5)] 

    Renal ToxicityInstruct patients experiencing decreased urinary output or other signs and symptoms of renal toxicity to immediately contact their healthcare provider [ seeWarnings and Precautions (5.6)].

    Serious Skin Toxicities

    Instruct patients skin rash, blistering, or peeling to immediately contact their healthcare provider [ see Warnings and Precautions (5.7)].

    Palmar-Plantar Erythrodysesthesia Syndrome

    Instruct patients experiencing grade 2 palmar-plantar erythrodysesthesia syndrome or greater to stop taking capecitabine immediately and to contact their healthcare provider. Inform patients that initiation of symptomatic treatment is recommended and hand-and-foot syndrome can lead to loss of fingerprints which could impact personal identification [ see Warnings and Precautions (5.8)].

    Myelosuppression

    Inform patients who develop a fever of 100.5°F or greater or other evidence of potential infection to immediately contact their healthcare provider [ see Warnings and Precautions (5.9)].

    Hyperbilirubinemia

    Inform patients who develop jaundice or icterus to immediately contact their healthcare provider [ see Warnings and Precautions (5.10)].

    Embryo-Fetal Toxicity

    Advise pregnant women and females of reproductive potential of the potential risk to a fetus. Advise females of reproductive potential to inform their healthcare provider of a known or suspected pregnancy [ see Warnings and Precautions (5.11), Use in Specific Populations (8.1)].

    Advise females of reproductive potential to use effective contraception during treatment with capecitabine and for 6 months after the last dose [ see Use in Specific Populations (8.3)].

    Advise males with female partners of reproductive potential to use effective contraception during treatment with capecitabine and for 3 months after the last dose [ see Use in Specific Populations (8.3)].

    Lactation

    Advise females not to breastfeed during treatment with capecitabine and for 1 week after the last dose [ see Use in Specific Populations (8.2)].

    Infertility

    Advise males and females of reproductive potential that capecitabine may impair fertility [ see Use in Specific Populations (8.3)].

    Hypersensitivity and Angioedema

    Advise patients that capecitabine may cause severe hypersensitivity reactions and angioedema. Advise patients who have known hypersensitivity to capecitabine or 5-fluorouracil to inform their healthcare provider [see Contraindications (4)]. Instruct patients who develop hypersensitivity reactions or mucocutaneous symptoms (e.g., urticaria, rash, erythema, pruritus, or swelling of the face, lips, tongue or throat which make it difficult to swallow or breathe) to stop taking capecitabine and immediately contact their healthcare provider or to go to an emergency room . [see Adverse Reactions (6)].

    Nausea and Vomiting

    Instruct patients experiencing grade 2 nausea (food intake significantly decreased but able to eat intermittently) or greater to stop taking capecitabine and to immediately contact their healthcare provider for management of nausea [see Adverse Reactions (6.1)].
    Instruct patients experiencing grade 2 vomiting (2 to 5 episodes in a 24-hour period) or greater to stop taking capecitabine immediately and to contact their healthcare provider for management of vomiting [see Adverse Reactions (6.1)].

    Stomatitis

    Inform patients experiencing grade 2 stomatitis (painful erythema, edema or ulcers of the mouth or tongue, but able to eat) or greater to stop taking capecitabine immediately and to contact their healthcare provider [see Adverse Reactions (6.1)].

    Important Administration Instructions

    Advise patients to swallow capecitabine tablets whole with water within 30 minutes after a meal. Advise patients and caregivers not to chew, crush, or cut capecitabine tablets. Advise patients if they cannot swallow capecitabine tablets whole to inform their healthcare provider [ see Dosage and Administration (2.7), Warnings and Precautions (5.12)].

    Drug interactions

    Instruct patients not to take products containing folic acid or folate analog products (e.g., leucovorin, levoleucovorin) unless directed to do so by their healthcare provider. Advise patients to inform their healthcare provider of all prescription or nonprescription medications, vitamins or herbal products [ see Drug Interactions (7.1, 7.2, 7.3)].

  • SPL UNCLASSIFIED SECTION

    Manufactured For:  

    Chartwell RX, LLC.

    Congers, NY 10920


    Manufactured by:

    Reliance Life Sciences Pvt. Ltd.

    Navi Mumbai - 400 701, INDIA

    L71747
    Rev. 10/2023

    Print Patient Information at: www.chartwellpharma.com/our-products/


    Print Patient Information at: www.chartwellpharma.com/our-products/

  • Patient Information

    CAPECITABINE (ka-pe-SITE-a-been) Tablets, USP 

    What is the most important information I should know about capecitabine tablets?

    Capecitabine tablets can cause serious side effects, including:

    • Increased risk of bleeding when taking capecitabine tablets with blood thinner medicines, such as warfarin. Taking capecitabine tablets with these medicines can cause changes in how fast your blood clots and can cause bleeding that can lead to death.This can happen as soon as a few days after you start taking capecitabine tablets, or later during treatment, and possibly within 1 month after you stop taking capecitabine tablets. This can happen in people whose cancer has spread to the liver (liver metastasis) andin people whose cancer has not spread to the liver.
      • Before taking capecitabine tablets, tell your healthcare provider if you are taking warfarin or another blood thinner medicine.
      • If you take warfarin or another blood thinner that is like warfarin during treatment with capecitabine tablets, your healthcare provider should do blood tests more often, to check how fast your blood clots during and after you stop treatment with capecitabine tablets. Your healthcare provider may change your dose of the blood thinner medicine if needed.
      • Tell your healthcare provider right away if you develop any signs or symptoms of bleeding.

    See “What are the possible side effects of capecitabine tablets?”for more information about side effects.  

    What are capecitabine tablets?

    Capecitabine tablets are prescription medicine used to treat: 

    • A kind of cancer called colon or rectal (colorectal) cancer. Capecitabine tablets may be used:
      • alone or in combination with other chemotherapy medicines in people with colon cancer that has spread to lymph nodes in the area close to the colon (Stage III colon cancer), to help prevent your cancer from coming back after you have had surgery.
      • adults with rectal cancer, around the time of your surgery, as a part of chemotherapy and radiation (chemoradiation) treatment when your rectal cancer has spread to nearby tissues (locally advanced).
      • alone or in combination with other chemotherapy medicines, when your colorectal cancer cannot be removed by surgery or has spread to other areas of your body (metastatic).
    • A kind of cancer called breast cancer. Capecitabine tablets may be used in people with breast cancer that is advanced or has spread to other parts of the body (metastatic):
      • alone if you are not able to receive an anthracycline medicine or taxane-containing chemotherapy.
      • in combination with docetaxel when you have received anthracycline containing chemotherapy and it is no longer working.
    • Kinds of cancer called stomach (gastric), esophageal, or gastroesophageal junction (GEJ) cancer. Capecitabine tablets may be used in adults:
      • in combination with other chemotherapy medicines when your cancer of the stomach, esophagus, or GEJ cannot be removed by surgery or has spread to other parts of the body (metastatic).
      • when your cancer of the stomach, esophagus, or GEJ is metastatic adenocarcinoma, and
        • is HER2-positive, and 
        • you have not received treatment with capecitabine tablets in combination with other treatments for your metastatic cancer
        • A kind of  cancer called pancreatic cancer. Capecitabine tablets may be used to treat adults in combination with other chemotherapy medicines, to help prevent your pancreatic cancer from coming back after you have had surgery.

    It is not known if capecitabine tablets are safe and effective in children.  

    Do not take capecitabine tablets if you:

    • have had a severe allergic reaction to fluorouracil or capecitabine. See the end of this leaflet for a complete list of ingredients in capecitabine tablets.

    Talk to your healthcare provider before taking capecitabine tablets if you are not sure.  

    Before taking capecitabine tablets, tell your healthcare provider about all your medical conditions, including if you: 

    See “ What is the most important information I should know about capecitabine tablets?”

    • have had heart problems
    • have kidney or liver problems
    • are pregnant or plan to become pregnant. Capecitabine tablets can harm your unborn baby.

    Females who are able to become pregnant

    • Your healthcare provider should do a pregnancy test before you start treatment with capecitabine tablets.
    • Use an effective method of birth control (contraception) during treatment and for 6 months after your last dose of capecitabine tablets. Talk to your healthcare provider about birth control choices that may be right for you during treatment with capecitabine tablets.
    • Tell your healthcare provider right away if you become pregnant or think you might be pregnant during treatment with capecitabine tablets.

    Maleswho have female partners who are able to become pregnant should use effective birth control during treatment and for 3 months after your last dose of capecitabine tablets.

    • are breastfeeding or plan to breastfeed. It is not known if capecitabine tablets passes into your breast milk. Do not breastfeed during treatment with capecitabine tablets and for 1 week after your last dose of capecitabine tablets.

    Tell your healthcare provider about all the medicines you take, including prescription and over the-counter medicines, vitamins, and herbal supplements. Capecitabine tablets may affect the way other medicines work, and other medicines may affect the way capecitabine tablets works.  

    How should I take capecitabine tablets?

    • Take capecitabine tablets exactly as your healthcare provider tells you to take it.
    • Your healthcare provider will tell you how much capecitabine tablets to take and when to take it. The number of days that you will take capecitabine tablets during each treatment cycle and the number of days in each treatment cycle depends on the type of cancer you are being treated for.
    • Take capecitabine tablets 2 times a day at the same time each day, about 12 hours apart.
    • Take capecitabine tablets within 30 minutes after finishing a meal.
    • Swallow capecitabine tablets whole with water. Do notchew, cut, or crush capecitabine tablets. See “Eye irritation, skin rash and other side effects with exposure to crushed capecitabine tablets” in the section called “What are the possible side effects of capecitabine tablets?”
    • If you cannot swallow capecitabine tablets whole, tell your healthcare provider.
    • Your healthcare provider may change your dose, temporarily stop, or permanently stop treatment with capecitabine tablets if you develop side effects.
    • Do nottake products that contain folic acid or folate analog products, for example, leucovorin or levoleucovorin, during treatment with capecitabine tablets, unless your healthcare provider instructs you to take it.
    • If you vomit after taking a dose of capecitabine tablets, do not take another dose at that time. Wait and take your next dose of capecitabine tablets at your scheduled time.
    • If you miss a dose of capecitabine tablets, just skip the dose and then take your next dose at your scheduled time.
    • If you take too much capecitabine tablets, call your healthcare provider or go to the nearest hospital emergency room right away.

    What are the possible side effects of capecitabine tablets? 

    Capecitabine tablets may cause serious side effects including: 

    • See “What is the most important information I should know about capecitabine tablets?”
    • Serious side effects in people with dihydropyrimidine dehydrogenase (DPD) enzyme deficiency.People with certain changes in a gene called “DPYD” may have a deficiency of the DPD enzyme. Some of these people may not produce enough DPD enzyme, and some of these people may not produce the DPD enzyme at all.
      • People who do not produce any DPD enzyme are at increased risk of sudden side effects that come on early during treatment with capecitabine tablets and can be serious, and sometimes lead to death. Call your healthcare provider right away if you develop any of the following symptoms and they are severe,including:
        • sores of the mouth, tongue, throat and esophagus (mucositis)
        • diarrhea                                         low white blood cell counts
        • nervous system problems.
      • People with some DPD enzyme may have an increased risk of serious side effects with capecitabine tablets treatment that can sometimes lead to death.

    Your healthcare provider should talk with you about DPYD testing to look for DPD deficiency.

    • Heart problems.Capecitabine tablets can cause heart problems including: heart attack and decreased blood flow to the heart, chest pain, irregular heartbeats, changes in the electrical activity of your heart seen on an electrocardiogram (ECG), problems with your heart muscle, heart failure, and sudden death. You may have an increased risk of heart problems with capecitabine tablets if you have a history of narrowing or blockage of the coronary arteries (coronary artery disease). Stop taking capecitabine tablets and call your healthcare provider or go to the nearest hospital emergency room right away if you get any new symptoms of a heart problem including:
      •        chest pain                                                        ○ dizziness
      •        shortness of breath                                         ○ lightheadedness
    • Diarrhea. Diarrhea is common with capecitabine tablets and can sometimes be severe. Stop taking capecitabine tablets and call your healthcare provider right away if the number of bowel movements you have in a day increases by 4 or more bowel movements than what is usual for you, or if you have bowel movements at night. Ask your healthcare provider about what medicines you can take to treat your diarrhea. Stop taking capecitabine tablets if you have severe bloody diarrhea with severe abdominal pain and fever and call you healthcare provider right away.
    • Loss of too much body fluid (dehydration) and kidney failure.Dehydration can happen with capecitabine tablets and may affect how well your kidneys work. If you take capecitabine tablets with certain other medicines that can cause kidney problems, you may have an increased risk of serious kidney failure that can sometimes lead to death. Your risk of kidney failure may also be increased if you have kidney problems before taking capecitabine tablets.

    Nausea, and vomiting are common with capecitabine tablets. If you lose your appetite, feel weak, and have nausea, vomiting, or diarrhea, you can quickly become dehydrated. 

    Stop taking capecitabine tablets and call your healthcare provider right away if you:

    • vomit 2 or more times in a day.
    • are only able to eat or drink a little now and then, or not at all due to nausea.
    • have diarrhea. See “diarrhea” above.

    You may need to receive fluids through your vein (intravenous) to treat your dehydration or receive treatment for kidney failure.

    • Severe skin and mouth reactions.
      • Capecitabine tablets can cause severe skin reactions that may lead to death. Tell your healthcare provider right away if you develop a skin rash, blister and peeling of your skin. Your healthcare provider may tell you to stop taking capecitabine tablets if you have a serious skin reaction. Do not take capecitabine tablets again if this happens. 
      • Capecitabine tablets can also cause “hand and foot” syndrome. Hand and foot syndrome is common with capecitabine tablets and can cause you to have numbness and changes in sensation in your hands and feet, or cause redness, pain, swelling of your hands and feet. Stop taking capecitabine tablets and call your healthcare provider right away if you have any of these symptoms and you are not able to do your usual activities.
      • Hand and foot syndrome can lead to a loss of fingerprints which could impact your identification.
      • You may get sores in your mouth or on your tongue when taking capecitabine tablets. Stop taking capecitabine tablets and call your healthcare provider right away if you get painful redness, swelling, or ulcers in your mouth or tongue, or if you are having problems eating. 
    • Decreased white blood cells, platelets, and red blood cell counts. Decreased white blood cells, platelets, and red blood cell counts can happen with capecitabine tablets and can sometimes be severe.
      Your healthcare provider will do blood tests during treatment with capecitabine tablets to check your blood cell counts.
      If your white blood cell count is very low, you are at increased risk for infection. Call your healthcare provider right away if you develop a fever of 100.5 oF or greater or have other signs and symptoms of infection.
    • Increased level of bilirubin in your blood and liver problems.Increased bilirubin in your blood is common with capecitabine tablets and can also sometimes be severe. Your healthcare provider will check you for these problems during treatment with capecitabine tablets. Tell your healthcare provider right away if you develop yellowing of your skin or the white part of your eyes.
    • Eye irritation, skin rash and other side effects with exposure to crushed capecitabine tablets.If you come into contact with (you are exposed to) crushed capecitabine tablets, you may develop side effects including: 
      • eye irritation and swelling           o feeling like pins and needles in your hands
      • skin rash                                       o headache
      • diarrhea                                        o stomach irritation
      • nausea and vomiting

    Do not chew, cut, or crush capecitabine tablets.See “How should I take capecitabine tablets.”

    If for any reason your tablets must be cut or crushed, this must be done by your pharmacist or healthcare provider.

    Your healthcare provider may decide to decrease your dose, or temporarily or permanently stop capecitabine tablets if you have serious side effects with capecitabine tablets.

    The most common side effects in people with colon cancer who take capecitabine tablets alone to help prevent it from coming back include: hand and foot syndrome, diarrhea, and nausea.

    The most common side effects in people with metastatic colorectal carcinoma who take capecitabine tablets alone include:

               decreased red blood cell count

               diarrhea                                                       nausea

               hand and foot syndrome                             tiredness

               increased bilirubin level in your blood       stomach-area (abdominal) pain

    The most common side effects in people with metastatic breast cancer who take capecitabine tablets in combination with docetaxel include:

              diarrhea                                                        hair loss

              mouth sores or mouth inflammation          swelling

              hand and foot syndrome                             stomach-area (abdominal) pain

              nausea and vomiting

    The most common side effects in people with metastatic breast cancer who take capecitabine tablets alone include:

            decreased white blood cell and red blood cell count               nausea and vomiting                               
            diarrhea                                                                                     tiredness                                                
            hand and foot syndrome                                                          skin inflammation, including rash

    Severe allergic reactions can happen with capecitabine tablets.See “Do not take capecitabine tablets if you:” Stop taking capecitabine tablets and call your healthcare provider right away or go to an emergency room if you have any of the following symptoms of a severe allergic reaction to capecitabine tablets:
              red itchy welts on your skin (hives)                   skin redness           swelling of your face, lips, tongue or throat     
              rash                                                                     itching                      trouble swallowing or breathing 

    Capecitabine tablets may cause fertility problems in females and males. This may affect the ability to have a child. Talk to your healthcare provider if you have concerns about fertility.

    These are not all the possible side effects of capecitabine tablets.

    Call your doctor for medical advice about side effects.
    You may report side effects to FDA at 1-800-FDA-1088

    How should I store capecitabine tablets?

    • Store capecitabine tablets at room temperature between 68°F to 77°F (20°C to 25°C).  
    • Keep capecitabine Tablets in a tightly closed container.
    • Ask your healthcare provider or pharmacist how to safely throw away any unused capecitabine.

     Keep capecitabine tablets and all medicines out of reach of children.

    General information about the safe and effective use of capecitabine tablets.

    Medicines are sometimes prescribed for conditions that are not mentioned in a Patient Information leaflets. Do not use capecitabine tablets for a condition for which it was not prescribed. Do not give capecitabine tablets to other people, even if they have the same symptoms you have. It may harm them. You can ask your pharmacist or healthcare provider for information about capecitabine tablets that are written for health professionals. 

    What are the ingredients in capecitabine tablets?

    Active ingredient: capecitabine  

    Inactive ingredients: anhydrous lactose, croscarmellose sodium, hydroxypropyl methylcellulose, microcrystalline cellulose, magnesium stearate. The peach or light peach film coating contains hydroxypropyl methylcellulose, polyethylene glycol, red iron oxides, synthetic yellow, talc and titanium dioxide.

    For more information, call Chartwell RX, LLC at 1-845-232-1683.

    All brand names listed are the registered trademarks of their respective owners and are not trademarks of Chartwell RX, LLC


    Manufactured by: 

    Reliance Life Sciences Pvt. Ltd.

    Navi Mumbai - 400 701, INDIA


    Manufactured For:

    Chartwell RX, LLC.

    Congers, NY 10920

    This Patient Information has been approved by the U.S. Food and Drug Administration.

    Rev.10/2023
    L71748

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Capecitabine Tablets, USP 150 mg - NDC: 62135-783-60 - 60's Bottle Label

    image description

    Capecitabine Tablets, USP 500 mg - NDC 62135-784-12 - 120's Bottle Label

    image description

  • INGREDIENTS AND APPEARANCE
    CAPECITABINE 
    capecitabine tablet
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 62135-783
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAPECITABINE (UNII: 6804DJ8Z9U) (CAPECITABINE - UNII:6804DJ8Z9U) CAPECITABINE150 mg
    Inactive Ingredients
    Ingredient NameStrength
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    TALC (UNII: 7SEV7J4R1U)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)  
    HYPROMELLOSE 2208 (3 MPA.S) (UNII: 9H4L916OBU)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    Product Characteristics
    Colorpink (Light Peach) Scoreno score
    ShapeOVAL (oblong) Size11mm
    FlavorImprint Code C150
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 62135-783-6060 in 1 BOTTLE; Type 0: Not a Combination Product10/16/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA21172404/27/2020
    CAPECITABINE 
    capecitabine tablet
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 62135-784
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAPECITABINE (UNII: 6804DJ8Z9U) (CAPECITABINE - UNII:6804DJ8Z9U) CAPECITABINE500 mg
    Inactive Ingredients
    Ingredient NameStrength
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    TALC (UNII: 7SEV7J4R1U)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)  
    HYPROMELLOSE 2208 (3 MPA.S) (UNII: 9H4L916OBU)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    Product Characteristics
    Colorpink (Peach) Scoreno score
    ShapeOVAL (Oblong) Size16mm
    FlavorImprint Code C500
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 62135-784-12120 in 1 BOTTLE; Type 0: Not a Combination Product10/16/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA21172404/27/2020
    Labeler - Chartwell RX, LLC (079394054)
    • © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.