DOXORUBICIN HYDROCHLORIDE injection, powder, lyophilized, for solution

Doxorubicin Hydrochloride by

Drug Labeling and Warnings

Doxorubicin Hydrochloride by is a Prescription medication manufactured, distributed, or labeled by Hikma Pharmaceuticals USA Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • BOXED WARNING (What is this?)

    WARNING: CARDIOMYOPATHY, SECONDARY MALIGNANCIES,EXTRAVASATION AND TISSUE NECROSIS, and SEVERE MYELOSUPPRESSION

    • Cardiomyopathy: Myocardial damage, including acute left ventricular failure can occur with doxorubicin. The risk of cardiomyopathy is proportional to the cumulative exposure with incidences from 1% to 20% for cumulative doses from 300 mg/m2 to 500 mg/m2 when doxorubicin is administered every 3 weeks. The risk of cardiomyopathy is further increased with concomitant cardiotoxic therapy. Assess LVEF before and regularly during and after treatment with doxorubicin [see Warnings and Precautions (5.1)].
    • Secondary Malignancies: Secondary acute myelogenous leukemia (AML) and myelodysplastic syndrome (MDS) occur at a higher incidence in patients treated with anthracyclines, including doxorubicin [see Warnings and Precautions (5.2)].
    • Extravasation and Tissue Necrosis: Extravasation of doxorubicin can result in severe local tissue injury and necrosis requiring wide excision of the affected area and skin grafting. Immediately terminate the drug, and apply ice to the affected area [see Warnings and Precautions (5.3)].
    • Severe myelosuppression resulting in serious infection, septic shock, requirement for transfusions, hospitalization, and death may occur [see Warnings and Precautions (5.4)].
  • 1 INDICATIONS AND USAGE

    1.1 Adjuvant Breast Cancer

    DOXOrubicin HCl for Injection, USP is indicated as a component of multi-agent adjuvant chemotherapy for treatment of women with axillary lymph node involvement following resection of primary breast cancer [see Clinical Studies (14.1)].

    1.2 Other Cancers

    Doxorubicin is indicated for the treatment of

    • acute lymphoblastic leukemia
    • acute myeloblastic leukemia
    • Hodgkin lymphoma
    • non-Hodgkin lymphoma (NHL)
    • metastatic breast cancer
    • metastatic Wilms’ tumor
    • metastatic neuroblastoma
    • metastatic soft tissue sarcoma
    • metastatic bone sarcoma
    • metastatic ovarian carcinoma
    • metastatic transitional cell bladder carcinoma
    • metastatic thyroid carcinoma
    • metastatic gastric carcinoma
    • metastatic bronchogenic carcinoma
  • 2 DOSAGE AND ADMINISTRATION

    2.1 Recommended Dose

    Adjuvant Breast Cancer

    The recommended dose of doxorubicin is 60 mg/m2 administered as an intravenous bolus on day 1 of each 21 day treatment cycle, in combination with cyclophosphamide, for a total of four cycles [see Clinical Studies (14)].

    Metastatic Disease, Leukemia, or Lymphoma

    • The recommended dose of doxorubicin when used as a single agent is 60 to 75 mg/m2 intravenously every 21 days.
    • The recommended dose of doxorubicin, when administered in combination with other chemotherapy drugs, is 40 to 75 mg/m2 intravenously every 21 to 28 days.
    • Consider use of the lower doxorubicin dose in the recommended dose range or longer intervals between cycles for heavily pretreated patients, elderly patients, or obese patients.
    • Cumulative doses above 550 mg/m2 are associated with an increased risk of cardiomyopathy [see Warnings and Precautions (5.1)].

    2.2 Dose Modifications

    Cardiac Impairment

    Discontinue doxorubicin in patients who develop signs or symptoms of cardiomyopathy.

    Hepatic Impairment

    Doxorubicin is contraindicated in patients with severe hepatic impairment (Child-Pugh Class C or serum bilirubin >5.0 mg/dL) [see Contraindications (4)].

    Decrease the dose of doxorubicin in patients with elevated serum total bilirubin concentrations as follows:

     

    Serum bilirubin concentration

    		 

    Doxorubicin Dose reduction

     

    1.2 to 3 mg/dL

    		 

    50 %

     

    3.1 to 5 mg/dL

    		 

    75 %

     

    greater than 5 mg/dL

    		 

    Do not initiate doxorubicin

    Discontinue doxorubicin

    [see Warnings and Precautions (5.5) and Use in Specific Population (8.7)]

    2.3 Preparation and Administration

    Preparation of DOXOrubicin HCl for Injection, USP;

    Reconstitute doxorubicin hydrochloride for injection with 0.9% Sodium Chloride Injection to obtain a final concentration of 2 mg per mL as follows:

    • 5 mL 0.9% Sodium Chloride Injection to reconstitute 10 mg doxorubicin HCl vial
    • 25 mL 0.9% Sodium Chloride Injection to reconstitute 50 mg doxorubicin HCl vial

    Gently shake vial until the contents have dissolved.

    Protect reconstituted solution from light.

    Administration

    Visually inspect parenteral drug products for particulate matter and discoloration prior to administration, whenever solution and container permit. Discard if the solution is discolored, cloudy, or contains particulate matter.

    Storage of vials of DOXOrubicin HCl for Injection, USP following reconstitution under refrigerated conditions can result in the formation of a gelled product. Place gelled product at room temperature [15º to 30ºC (59º to 86ºF)] for 2 to 4 hours to return the product to a slightly viscous, mobile solution.

    Administration by Intravenous Injection:

    • Administer doxorubicin  as an intravenous injection  through a central intravenous line or a secure and free-flowing peripheral venous line containing 0.9% Sodium Chloride Injection, 0.45% Sodium Chloride Injection, or 5% Dextrose Injection. 
    • Administer doxorubicin intravenously over 3 to 10 minutes. Decrease the rate of doxorubicin administration if erythematous streaking along the vein proximal to the site of infusion or facial flushing occur.

    Administration by Continuous Intravenous Infusion:

    • Infuse only through a central catheter. Decrease the rate of doxorubicin administration if erythematous streaking along the vein proximal to the site of infusion or facial flushing occur.
    • Protect from light from preparation for infusion until completion of infusion.

    Management of Suspected Extravasation

    Discontinue doxorubicin for burning or stinging sensation or other evidence indicating peri­venous infiltration or extravasation. Manage confirmed or suspected extravasation as follows:

    • Do not remove the needle until attempts are made to aspirate extravasated fluid.
    • Do not flush the line.
    • Avoid applying pressure to the site.
    • Apply ice to the site intermittently for 15 min 4 times a day for 3 days.
    • If the extravasation is in an extremity, elevate the extremity.
    • In adults, consider administration of dexrazoxane [see Warnings and Precautions (5.3)].

    Incompatibility with Other Drugs

    Do not admix doxorubicin with other drugs. If doxorubicin is mixed with heparin or fluorouracil a precipitate may form. Avoid contact with alkaline solutions which can lead to hydrolysis of doxorubicin.

    2.4 Procedures for Proper Handling and Disposal

    Handle and dispose of doxorubicin consistent with recommendations for the handling and disposal of hazardous drugs.1

    Treat accidental contact with the skin or eyes immediately by copious lavage with water, or soap and water, or sodium bicarbonate solution. Do not abrade the skin by using a scrub brush. Seek medical attention.

  • 3 DOSAGE FORMS AND STRENGTHS

    DOXOrubicin HCl for Injection, USP: Vials contain 10 mg and 50 mg doxorubicin hydrochloride as a red-orange lyophilized powder.

  • 4 CONTRAINDICATIONS

    Doxorubicin is contraindicated in patients with:

  • 5 WARNINGS AND PRECAUTIONS

    5.1 Cardiomyopathy and Arrhythmias

    Cardiomyopathy

    Doxorubicin can result in myocardial damage, including acute left ventricular failure. The risk of cardiomyopathy is generally proportional to the cumulative exposure. Include prior doses of other anthracyclines or anthracenediones in calculations of total cumulative dosage for doxorubicin. Cardiomyopathy may develop during treatment or up to several years after completion of treatment and can include decrease in LVEF and signs and symptoms of congestive heart failure (CHF). The probability of developing cardiomyopathy is estimated to be 1 to 2% at a total cumulative dose of 300 mg/m2 of doxorubicin, 3 to 5% at a dose of 400 mg/m2, 5 to 8% at a dose of 450 mg/m2, and 6 to 20% at a dose of 500 mg/m2, when doxorubicin is administered every 3 weeks. There is an additive or potentially synergistic increase in the risk of cardiomyopathy in patients who have received radiotherapy to the mediastinum or concomitant therapy with other known cardiotoxic agents such as cyclophosphamide and trastuzumab.

    Pericarditis and myocarditis have also been reported during or following doxorubicin treatment.

    Assess left ventricular cardiac function (e.g., MUGA or echocardiogram) prior to initiation of doxorubicin, during treatment to detect acute changes, and after treatment to detect delayed cardiotoxicity. Increase the frequency of assessments as the cumulative dose exceeds 300 mg/m2 . Use the same method of assessment of LVEF at all time points [see Use in Specific Populations (8.4)].

    Consider the use of dexrazoxane to reduce the incidence and severity of cardiomyopathy due to doxorubicin administration in patients who have received a cumulative doxorubicin dose of 300 mg/m2 and who will continue to receive doxorubicin.

    Arrhythmias

    Doxorubicin can result in arrhythmias, including life-threatening arrhythmias, during or within a few hours after doxorubicin administration and at any time point during treatment. Tachyarrhythmias, including sinus tachycardia, premature ventricular contractions, and ventricular tachycardia, as well as bradycardia may occur. Electrocardiographic changes including non-specific ST-T wave changes, atrioventricular and bundle-branch block can also occur. These electrocardiographic changes may be transient and self-limited and may not require dose-modifications of doxorubicin.

    5.2 Secondary Malignancies

    The risk of developing secondary acute myelogenous leukemia (AML) and myelodysplastic syndrome (MDS) is increased following treatment with doxorubicin. Cumulative incidences ranged from 0.2% at five years to 1.5% at 10 years in two separate trials involving the adjuvant treatment of women with breast cancer. These leukemias generally occur within 1 to 3 years of treatment.

    5.3 Extravasation and Tissue Necrosis

    Extravasation of doxorubicin can result in severe local tissue injury manifesting as blistering, ulceration, and necrosis requiring wide excision of the affected area and skin grafting. When given via a peripheral venous line, infuse doxorubicin over 10 minutes or less to minimize the risk of thrombosis or perivenous extravasation. If signs or symptoms of extravasation occur, immediately terminate the injection or infusion [see Dosage and Administration (2.3)]. Extravasation may be present in patients who do not experience a stinging or burning sensation or when blood return is present on aspiration of the infusion needle. If extravasation is suspected, apply ice to the site intermittently for 15 minutes, 4 times a day for 3 days. If appropriate, administer dexrazoxane at the site of extravasation as soon as possible and within the first 6 hours after extravasation.

    5.4 Severe Myelosuppression

    Doxorubicin can cause myelosuppression. In Study 1, the incidence of severe myelosuppression was: grade 4 leukopenia (0.3%), grade 3 leukopenia (3%), and grade 4 thrombocytopenia (0.1%). A dose-dependent, reversible neutropenia is the predominant manifestation of hematologic toxicity from doxorubicin. When doxorubicin is administered every 21 days, the neutrophil count reaches its nadir 10 to 14 days after administration with recovery usually occurring by the 21st day.

    Obtain baseline assessment of blood counts and carefully monitor patients during treatment for possible clinical complications due to myelosuppression.

    5.5 Use in Patients with Hepatic Impairment

    The clearance of doxorubicin is decreased in patients with elevated serum bilirubin with an increased risk of toxicity [see Use in Specific Populations (8.7) and Clinical Pharmacology (12.3)]. Reduce the dose of doxorubicin in patients with serum bilirubin levels of 1.2 to 5.0 mg/dL [see Dosage and Administration (2.2)]. Doxorubicin is contraindicated in patients with severe hepatic impairment (defined as Child Pugh Class C or serum bilirubin level greater than 5 mg/dL) [see Contraindications (4)]. Obtain liver tests including SGOT, SGPT, alkaline phosphatase, and bilirubin prior to and during doxorubicin therapy.

    5.6 Tumor Lysis Syndrome

    Doxorubicin may induce tumor lysis syndrome in patients with rapidly growing tumors. Evaluate blood uric acid levels, potassium, calcium, phosphate, and creatinine after initial treatment. Hydration, urine alkalinization, and prophylaxis with allopurinol to prevent hyperuricemia may minimize potential complications of tumor lysis syndrome.

    5.7 Radiation Sensitization and Radiation Recall

    Doxorubicin can increase radiation-induced toxicity to the myocardium, mucosa, skin, and liver. Radiation recall, including but not limited to cutaneous and pulmonary toxicity, can occur in patients who receive doxorubicin after prior radiation therapy.

    5.8 Embryofetal Toxicity

    Doxorubicin can cause fetal harm when administered to a pregnant woman. Doxorubicin was teratogenic and embryotoxic in rats and rabbits at doses lower than the recommended human dose.

    If this drug is used during pregnancy, or if the patient becomes pregnant while taking this drug, apprise the patient of the potential hazard to a fetus [see Use in Specific Populations (8.1)].

    Advise female patients of reproductive potential to use highly effective contraception during treatment with doxorubicin and for 6 months after treatment. Advise patients to contact their healthcare provider if they become pregnant, or if pregnancy is suspected, while taking doxorubicin [see Use in Specific Populations (8.1) and (8.6)].

  • 6 ADVERSE REACTIONS

    The following adverse reactions are discussed in more detail in other sections of the labeling.

    6.1 Clinical Trial Experience in Breast Cancer

    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 clinical practice.

    The safety data below were collected from 1492 women who received doxorubicin at a dose of 60 mg/m2 and cyclophosphamide at a dose of 600 mg/m2 (AC) every 3 weeks for 4 cycles for the adjuvant treatment of axillary lymph node positive breast cancer. The median number of cycles received was 4. Selected adverse reactions reported in this study are provided in Table 1. No treatment-related deaths were reported in patients on either arm of the study.

     

    Table 1. Selected Adverse Reactions in Patients with Early Breast Cancer Involving Axillary Lymph Nodes

     

    Adverse reactions, % of patients

    		 

    AC*

    N=1492

    		 

    Conventional CMF

    N=739

     

    Leukopenia

    Grade 3 (1,000 to 1,999 /mm3)

    Grade 4 (<1000 /mm3)

    		 

    3.4

    0.3

    		 

    9.4

    0.3
     

    Thrombocytopenia

    Grade 3 (25,000 to 49,999 /mm3)

    Grade 4 (<25,000 /mm3)

    		 

    0

    0.1

    		 

    3.0

    0
     

    Shock, sepsis

    		 

    2

    		 

    1
     

    Systemic infection

    		 

    2

    		 

    1
     

    Vomiting

    Vomiting ≤12 hours

    Vomiting >12 hours

    Intractable

    		 

    34

    37

    5

    		 

    25

    12

    2
     

    Alopecia

    		 

    92

    		 

    71
     

    Cardiac dysfunction

    Asymptomatic

    Transient

    Symptomatic

    		 

    0.2

    0.1

    0.1

    		 

    0.1

    0

    0

    * Includes pooled data from patients who received either AC alone for 4 cycles, or who were treated with AC for 4 cycles followed by 3 cycles of CMF

    6.2 Postmarketing Experience

    The following adverse reactions have been identified during post-approval use of doxorubicin. 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.

    Cardiac – cardiogenic shock

    Cutaneous – Skin and nail hyperpigmentation, oncolysis, rash, itching, photosensitivity, urticaria, acral erythema, palmar plantar erythrodysesthesia

    Gastrointestinal – Nausea, mucositis, stomatitis, necrotizing colitis, typhlitis, gastric erosions, gastrointestinal tract bleeding, hematochezia, esophagitis, anorexia, abdominal pain, dehydration, diarrhea, hyperpigmentation of the oral mucosa

    Hypersensitivity – Anaphylaxis

    Laboratory Abnormalities –Increased alanine aminotransferase, increased aspartate aminotransferase

    Neurological – Peripheral sensory and motor neuropathy, seizures, coma

    Ocular – Conjunctivitis, keratitis, lacrimation

    Vascular – Phlebosclerosis, phlebitis/thrombophlebitis, hot flashes, thromboembolism

    Other – Malaise/asthenia, fever, chills, weight gain

  • 7 DRUG INTERACTIONS

    7.1 Effect of CYP3A4 Inhibitors, Inducers and P-gp

    Doxorubicin is a major substrate of cytochrome P450 CYP3A4 and CYP2D6, and P-glycoprotein (P-gp). Clinically significant interactions have been reported with inhibitors of CYP3A4, CYP2D6, and/or P-gp (e.g., verapamil), resulting in increased concentration and clinical effect of doxorubicin. Inducers of CYP3A4 (e.g., phenobarbital, phenytoin, St. John’s Wort) and P-gp inducers may decrease the concentration of doxorubicin. Avoid concurrent use of doxorubicin with inhibitors and inducers of CYP3A4, CYP2D6, or P-gp.

    7.2 Trastuzumab

    Concurrent use of trastuzumab and doxorubicin results in an increased risk of cardiac dysfunction. Avoid concurrent administration of doxorubicin and trastuzumab. The appropriate interval for administering doxorubicin following trastuzumab therapy has not been determined [see Warnings and Precautions (5.1)].

    7.3 Paclitaxel

    Paclitaxel, when given prior to doxorubicin, increases the plasma-concentrations of doxorubicin and its metabolites. Administer doxorubicin prior to paclitaxel if used concomitantly.

    7.4 Dexrazoxane

    Do not administer dexrazoxane as a cardioprotectant at the initiation of doxorubicin containing chemotherapy regimens. In a randomized trial in women with metastatic breast cancer, initiation of dexrazoxane with doxorubicin based chemotherapy resulted in a significantly lower tumor response rate (48% vs. 63%; p=0.007) and shorter time to progression than in women who received doxorubicin based chemotherapy alone.

    7.5 6-Mercaptopurine

    Doxorubicin may potentiate 6-mercaptopurine-induced hepatotoxicity. In 11 patients with refractory leukemia treated with 6-mercaptopurine (500 mg/m2 intravenously daily for 5 days per cycle every 2 to 3 weeks) and doxorubicin (50 mg/m2 intravenous once per cycle every 2 to 3 weeks) alone or with vincristine and prednisone, all developed hepatic dysfunction manifested by elevations of total serum bilirubin, alkaline phosphatase and aspartate aminotransferase.

  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Pregnancy Category D

    Risk Summary

    Doxorubicin can cause fetal harm when administered to a pregnant woman. Doxorubicin was teratogenic and embryotoxic in rats and rabbits at doses approximately 0.07 times (based on body surface area) the recommended human dose of 60 mg/m2 . If this drug is used during pregnancy, or if the patient becomes pregnant while taking this drug, apprise the patient of the potential hazard to a fetus.

    Animal Data

    Doxorubicin was teratogenic and embryotoxic at doses of 0.8 mg/kg/day (about 0.07 times the recommended human dose based on body surface area) when administered during the period of organogenesis in rats. Teratogenicity and embryotoxicity were also seen using discrete periods of treatment. The most susceptible was the 6- to 9-day gestation period at doses of 1.25 mg/kg/day and greater. Characteristic malformations included esophageal and intestinal atresia, tracheo-esophageal fistula, hypoplasia of the urinary bladder, and cardiovascular anomalies. Doxorubicin was embryotoxic (increase in embryofetal deaths) and abortifacient at 0.4 mg/kg/day (about 0.07 times the recommended human dose based on body surface area) in rabbits when administered during the period of organogenesis.

    8.3 Nursing Mothers

    Doxorubicin has been detected in the milk of at least one lactating patient [see Clinical Pharmacology (12.3)]. Because of the potential for serious adverse reactions in nursing infants from doxorubicin , a decision should be made whether to discontinue nursing or discontinue the drug, taking into account the importance of the drug to the mother.

    8.4 Pediatric Use

    Based on postmarketing reports, pediatric patients treated with doxorubicin are at risk for developing late cardiovascular dysfunction. Risk factors include young age at treatment (especially < 5 years), high cumulative doses and receipt of combined modality therapy. Long-term periodic cardiovascular monitoring is recommended for all pediatric patients who have received doxorubicin. Doxorubicin, as a component of intensive chemotherapy regimens administered to pediatric patients, may contribute to prepubertal growth failure and may also contribute to gonadal impairment, which is usually temporary.

    There are no recommended dose adjustments based on age. Doxorubicin clearance was increased in patients aged 2 years to 20 years as compared to adults, while doxorubicin clearance was similar in children less than 2 years as compared to adults [see Clinical Pharmacology (12.3)].

    8.5 Geriatric Use

    Clinical experience in patients who were 65 years of age and older who received doxorubicin based chemotherapy regimens for metastatic breast cancer showed no overall differences in safety and effectiveness compared with younger patients.

    8.6 Females and Males of Reproductive Potential

    Contraception

    Females

    Doxorubicin can cause fetal harm when administered during pregnancy. Advise female patients of reproductive potential to use highly effective contraception during treatment with doxorubicin and for 6 months after treatment. Advise patients to contact their healthcare provider if they become pregnant, or if pregnancy is suspected, while taking doxorubicin [see Use in Specific Populations (8.1)].

    Males

    Doxorubicin may damage spermatozoa and testicular tissue, resulting in possible genetic fetal abnormalities. Males with female sexual partners of reproductive potential should use effective contraception during and for 6 months after treatment [see Nonclinical Toxicology (13.1)].

    Infertility

    Females

    In females of reproductive potential, doxorubicin may cause infertility and result in amenorrhea. Premature menopause can occur. Recovery of menses and ovulation is related to age at treatment [see Nonclinical Toxicology (13.1)].

    Males

    Doxorubicin may result in oligospermia, azoospermia, and permanent loss of fertility. Sperm counts have been reported to return to normal levels in some men. This may occur several years after the end of therapy.

    8.7 Hepatic Impairment

    The clearance of doxorubicin was reduced in patients with elevated serum bilirubin levels. Reduce the dose of doxorubicin in patients with serum bilirubin levels greater than 1.2 mg/dL [see Dosage and Administration (2.2) and Warnings and Precautions (5.5)].

    Doxorubicin is contraindicated in patients with severe hepatic impairment (defined as Child Pugh Class C or serum bilirubin levels greater than 5 mg/dL) [see Contraindications (4)].

  • 10 OVERDOSAGE

    Few cases of overdose have been described. A 58-year-old man with acute lymphoblastic leukemia received 10-fold overdose of doxorubicin (300 mg/m2) in one day. He was treated with charcoal filtration, hemopoietic growth factor (G-CSF), proton pump inhibitor and antimicrobial prophylaxis. The patient suffered sinus tachycardia, grade 4 neutropenia and thrombocytopenia for 11 days, severe mucositis and sepsis. The patient recovered completely 26 days after the overdose. A 17-year-old girl with osteogenic sarcoma received 150 mg of doxorubicin daily for 2 days (intended dose was 50 mg per day for 3 days). The patient developed severe mucositis on days 4 to 7 after the overdose and chills and pyrexia on day 7. The patient was treated with antibiotics and platelets and recovered 18 days after overdose.

  • 11 DESCRIPTION

    Doxorubicin is a cytotoxic anthracycline antibiotic isolated from cultures of Streptomyces peucetius var.caesius. Doxorubicin consists of a naphthacenequinone nucleus linked through a glycosidic bond at ring atom 7 to an amino sugar, daunosamine. Chemically, doxorubicin hydrochloride is (8S,10S)-10-[(3-Amino-2,3,6-trideoxy-a-L-lyxo-hexopyranosyl)-oxy]-8-glycoloyl-7,8,9,10-tetrahydro-6,8,11-trihydroxy-1-methoxy-5,12-naphthacenedione hydrochloride. The structural formula is as follows:

    structure

    Doxorubicin binds to nucleic acids, presumably by specific intercalation of the planar anthracycline nucleus with the DNA double helix. The anthracycline ring is lipophilic, but the saturated end of the ring system contains abundant hydroxyl groups adjacent to the amino sugar, producing a hydrophilic center. The molecule is amphoteric, containing acidic functions in the ring phenolic groups and a basic function in the sugar amino group. It binds to cell membranes as well as plasma proteins.

    It is supplied in the hydrochloride form as a sterile red-orange lyophilized powder containing lactose for intravenous use only.

    DOXOrubicin HCl for Injection, USP:

    Each 10 mg lyophilized vial contains 10 mg of Doxorubicin Hydrochloride, USP and 50 mg of Lactose Monohydrate, NF.

    Each 50 mg lyophilized vial contains 50 mg of Doxorubicin Hydrochloride, USP and 250 mg of Lactose Monohydrate, NF.

  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    The cytotoxic effect of doxorubicin on malignant cells and its toxic effects on various organs are thought to be related to nucleotide base intercalation and cell membrane lipid binding activities of doxorubicin. Intercalation inhibits nucleotide replication and action of DNA and RNA polymerases. The interaction of doxorubicin with topoisomerase II to form DNA-cleavable complexes appears to be an important mechanism of doxorubicin cytocidal activity.

    12.3 Pharmacokinetics

    Pharmacokinetic studies conducted in patients with various types of tumors have shown that doxorubicin follows multiphasic disposition after intravenous injection. The distribution half-life is approximately 5 minutes, while the terminal half-life is 20 to 48 hours. In four patients, doxorubicin demonstrated dose-independent pharmacokinetics across a dose range of 30 to 70 mg/m2 .

    Distribution

    Steady-state distribution volume ranges from 809 to 1214 L/m2. Binding of doxorubicin and its major metabolite, doxorubicinol, to plasma proteins is about 75% and is independent of plasma concentration of doxorubicin up to 1.1 mcg/mL.

    Doxorubicin was measured in the milk of one lactating patient after therapy with 70 mg/m2 of doxorubicin given as a 15 minute intravenous infusion. The peak milk concentration at 24 hours after treatment was 4.4 fold greater than the corresponding plasma concentration. Doxorubicin was detectable in the milk up to 72 hours.

    Doxorubicin does not cross the blood brain barrier.

    Metabolism

    Enzymatic reduction at the 7 position and cleavage of the daunosamine sugar yields aglycones which are accompanied by free radical formation, the local production of which may contribute to the cardiotoxic activity of doxorubicin. Disposition of doxorubicinol in patients is formation rate limited, with the terminal half-life of doxorubicinol being similar to doxorubicin. The relative exposure of doxorubicinol, i.e., the ratio between the AUC of doxorubicinol and the AUC of doxorubicin is approximately 0.5.

    Excretion

    Plasma clearance is in the range 324 to 809 mL/min/m2 and is predominately by metabolism and biliary excretion. Approximately 40% of the dose appears in the bile in 5 days, while only 5 to 12% of the drug and its metabolites appear in the urine during the same time period. In urine, <3% of the dose was recovered as doxorubicinol over 7 days.

    Systemic clearance of doxorubicin is significantly reduced in obese women with ideal body weight greater than 130%. There was a significant reduction in clearance without any change in volume of distribution in obese patients when compared with normal patients with less than 115% ideal body weight.

    Pediatric patients

    Following administration of doses ranging from 10 to 75 mg/m2 of doxorubicin to 60 children and adolescents ranging from 2 months to 20 years of age, doxorubicin clearance averaged 1443 ± 114 mL/min/m2. Further analysis demonstrated that clearance in 52 children greater than 2 years of age (1540 mL/min/m2) was increased compared with adults. However, clearance in infants younger than 2 years of age (813 mL/min/m2) was decreased compared with older children and approached the range of clearance values determined in adults [see Use in Specific Populations (8.4)].

    Patient Gender

    There is no recommended dose adjustment based on gender. A published clinical study involving 6 men and 21 women with no prior anthracycline therapy reported a significantly higher median doxorubicin clearance in men compared to women (1088 mL/min/m2 versus 433 mL/min/m2). However, the terminal half-life of doxorubicin was longer in men compared to women (54 versus 35 hours).

    Patients with hepatic impairment

    The clearance of doxorubicin and doxorubicinol was reduced in patients with elevation in serum bilirubin [see Dosage and Administration (2.2)  and Warnings and Precautions (5.5)].

  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    Doxorubicin treatment results in an increased risk of secondary malignancies based on postmarketing reports [see Warnings and Precautions (5.2)]. Doxorubicin was mutagenic in the in vitro Ames assay, and clastogenic in multiple in vitro assays (CHO cell, V79 hamster cell, human lymphoblast, and SCE assays) and the in vivo mouse micronucleus assay.

    Doxorubicin decreased fertility in female rats at the doses of 0.05 and 0.2 mg/kg/day (approximately 0.005 and 0.02 times the recommended human dose, based on body surface area)

    A single intravenous dose of 0.1 mg/kg doxorubicin (approximately 0.01 times the recommended human dose based on body surface area) was toxic to male reproductive organs in animal studies, producing testicular atrophy, diffuse degeneration of the seminiferous tubules, and oligospermia/hypospermia in rats. Doxorubicin induces DNA damage in rabbit spermatozoa and dominant lethal mutations in mice.

  • 14 CLINICAL STUDIES

    The clinical efficacy of doxorubicin containing regimens for the post-operative, adjuvant treatment of surgically resected breast cancer was evaluated in a meta-analysis conducted by the Early Breast Cancer Trialists Collaborative Group (EBCTCG). The EBCTCG meta-analyses compared cyclophosphamide, methotrexate, and 5-fluorouracil (CMF) to no chemotherapy (19 trials including 7523 patients) and doxorubicin containing regimens with CMF as an active control (6 trials including 3510 patients). Data from the meta-analysis of trials comparing CMF to no therapy were used to establish the historical treatment effect size for CMF regimens. The major efficacy outcome measures were disease-free survival (DFS) and overall survival (OS).

    Of the 3510 women (2157 received doxorubicin containing regimens and 1353 received CMF treatment) with early breast cancer involving axillary lymph nodes included in the six trials from the meta-analyses, approximately 70% were premenopausal and 30% were postmenopausal. At the time of the meta-analysis, 1745 first recurrences and 1348 deaths had occurred. The analyses demonstrated that doxorubicin containing regimens retained at least 75% of the historical CMF adjuvant effect on DFS with a hazard ratio (HR) of 0.91 (95% CI, 0.82 to 1.01 ) and on OS with a HR of 0.91 (95% CI, 0.81 to 1.03 ). Results of these analyses for both DFS and OS are provided in Table 2 and Figures 1 and 2.

    Table 2. Summary of Randomized Trials Comparing Doxorubicin Containing Regimens Versus CMF in Meta-Analysis

     

    Study (starting year)

    		 

    Regimens

    		 

    No. of Cycles

    		 

    No. of Patients

    		 

    Doxorubicin Containing Regimens vs. CMF HR** (95% CI)

     

    DFS

    		 

    OS

     

    NSABP B-15 (1984)

    		 

    AC

    CMF

    		 

    4

    6

    		 

    1562*

    776

    		 

    0.93 (0.82 to 1.06)

    		 

    0.97 (0.83 to 1.12)
     

    SECSG 2 (1976)

    		 

    FAC

    CMF

    		 

    6

    6

    		 

    260

    268

    		 

    0.86 (0.66 to 1.13)

    		 

    0.93 (0.69 to 1.26)
     

    ONCOFRANCE (1978)

    		 

    FACV

    CMF

    		 

    12

    12

    		 

    138

    113

    		 

    0.71 (0.49 to 1.03)

    		 

    0.65 (0.44 to 0.96)
     

    SE Sweden BCG A (1980)

    		 

    AC

    CMF

    		 

    6

    6

    		 

    21

    22

    		 

    0.59 (0.22 to 1.61)

    		 

    0.53 (0.21 to 1.37)
     

    NSABC Israel Br0283 (1983)

    		 

    AVbCMF†

    CMF

    		 

    4

    6

    6

    		 

    55

    50

    		 

    0.91 (0.53 to 1.57)

    		 

    0.88 (0.47 to 1.63)
     

    Austrian BCSG 3 (1984)

    		 

    CMFVA

    CMF

    		 

    6

    8

    		 

    121

    124

    		 

    1.07 (0.73 to 1.55)

    		 

    0.93 (0.64 to 1.35)
     

    Combined Studies

    		 

    Doxorubicin Containing Regimens CMF

    		 

    2157

    1353

    		 

    0.91 (0.82 to 1.01)

    		 

    0.91 (0.81 to 1.03)

    Abbreviations: DFS = disease free survival; OS = overall survival; AC = doxorubicin, cyclophosphamide; AVbCMF = doxorubicin, vinblastine, cyclophosphamide, methotrexate, 5-fluorouracil; CMF = cyclophosphamide, methotrexate, 5-fluorouracil; CMFVA = cyclophosphamide, methotrexate, 5-fluorouracil, vincristine, doxorubicin; FAC = 5-fluorouracil, doxorubicin, cyclophosphamide; FACV = 5-fluorouracil, doxorubicin, cyclophosphamide, vincristine; HR = hazard ratio; CI = confidence interval

    * Includes pooled data from patients who received either AC alone for 4 cycles, or who were treated with AC for 4
    cycles followed by 3 cycles of CMF.
    ** A hazard ratio of less than 1 indicates that the treatment with doxorubicin containing regimens is associated
    with lower risk of disease recurrences or death compared to the treatment with CMF.

    † Patients received alternating cycles of AVb and CMF.

    fig. 1
    fig. 2
  • 15 REFERENCES

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

  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    DOXOrubicin HCI for Injection, USP is supplied as a sterile red-orange lyophilized powder in single dose flip-top vials in the following package strengths:

    NDC: 0143-9092-01: 10 mg vial; individually boxed.

    NDC: 0143-9093-01: 50 mg vial; individually boxed.

    Store all vials at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Protect from light. Retain in carton until time of use. Discard unused portion.

    Reconstituted Solution Stability

    After adding the diluent, the vial should be shaken and the contents allowed to dissolve. The reconstituted solution is stable for 7 days at room temperature and under normal room light (100 foot-candles) and 15 days under refrigeration (2° to 8°C). It should be protected from exposure to sunlight. Discard any unused solution from the 10 mg and 50 mg single dose vials.

    Handling and Disposal

    Handle and dispose of DOXOrubicin HCl for Injection, USP consistent with recommendations for the handling and disposal of hazardous drugs.1 

  • 17 PATIENT COUNSELING INFORMATION

    See FDA-Approved Patient Labeling (Patient Information). Inform patients of the following:

    • Doxorubicin can cause irreversible myocardial damage. Advise patients to contact a healthcare provider for symptoms of heart failure during or after treatment with doxorubicin [see Warnings and Precautions (5.1)].
    • There is an increased risk of treatment-related leukemia from doxorubicin [see Warnings and Precautions (5.2)].
    • Doxorubicin can reduce the absolute neutrophil count resulting in an increased risk of infection. Advise patients to contact a healthcare provider for new onset fever or symptoms of infection [see Warnings and Precautions (5.4)].
    • Doxorubicin can cause fetal harm when administered during pregnancy. Advise females of reproductive potential to use effective contraception during treatment with doxorubicin and for 6 months after treatment, and to contact their healthcare provider if they become pregnant, or if pregnancy is suspected, during treatment with doxorubicin [see Warnings and Precautions (5.8) and Use in Specific Populations (8.6)].
    • Doxorubicin may induce chromosomal damage in sperm, which may lead to loss of fertility and offspring with birth defects. Advise patients to use effective contraception during and for 6 months after treatment [see Warnings and Precautions (5.8) and Use in Specific Populations (8.6)].
    • Doxorubicin can cause premature menopause in females and loss of fertility in males [see Use in Specific Populations (8.6)].
    • Discontinue nursing while receiving doxorubicin [see Use in Specific Populations (8.3)].
    • Doxorubicin can cause nausea, vomiting, diarrhea, mouth/oral pain and sores. Advise patients to contact a healthcare provider should they develop any severe symptoms that prevent them from eating and drinking [see Adverse Reactions (6)].
    • Doxorubicin causes alopecia [see Adverse Reactions (6.1)].
    • Doxorubicin can cause their urine to appear red for 1 to 2 days after administration.

    Manufactured by

    THYMOORGAN PHARMAZIE GmbH

    Schiffgraben 23, 38690 Goslar, Germany

    Distributed by

    Hikma Pharmaceuticals USA Inc.

    Berkeley Heights, NJ 07922

    Revised March 2021

    127.207.045/00

  • Patient Information

    DOXORUBICIN (dok-suh-roo-buh-sin) HYDROCHLORIDE for Injection, for intravenous use

    What is the most important information I should know about Doxorubicin? 

    Doxorubicin may cause serious side effects including:

    • Heart failure. Doxorubicin may cause heart muscle damage that may lead to heart failure, which is a condition in which the heart does not pump well. Heart failure is irreversible in some cases and can lead to death. Heart failure can happen during your treatment with Doxorubicin or months to years after stopping treatment. Your risk of heart muscle damage increases with higher total amounts of doxorubicin hydrochloride that you receive in your lifetime. Your risk of heart failure is higher if you:
      • already have other heart problems
      • have had or are currently receiving radiation therapy to your chest
      • have had treatment with certain other anti-cancer medicines
      • take other medicines that can have severe side effects on your heart

    Tell your doctor if you get any of these symptoms of heart failure during or after treatment with Doxorubicin:

    • extreme tiredness or
    • fast heartbeat weakness
    • swelling of your feet and ankles
    • shortness of breath

    Your doctor will do tests to check the strength of your heart muscle before, during, and after your treatment with Doxorubicin.

    • Risk of new cancers. You may have an increased risk of developing certain blood cancers called acute myelogenous leukemia (AML) or myelodysplastic syndrome (MDS) after treatment with doxorubicin. Talk with your doctor about your risk of developing new cancers if you take Doxorubicin.
    • Skin damage near the vein where Doxorubicin is given (Injection site reaction). Doxorubicin can damage the skin if it leaks out of the vein. Symptoms of infusion reaction include blisters and skin sores at injection site which may require skin grafts.
    • Decreased blood cell counts. Doxorubicin can cause a decrease in neutrophils (a type of white blood cells important in fighting bacterial infections) and platelets (important for clotting and to control bleeding). This may lead to a serious infection, the need for blood transfusions, treatment in a hospital and death. Your doctor will check your blood cell count during your treatment with Doxorubicin and after you have stopped your treatment. Call your doctor right away if you get a fever (temperature of 100.4°F or greater) or chills with shivering.

    What is Doxorubicin?

    Doxorubicin is a prescription medicine used to treat certain types of cancers. Doxorubicin may be used alone or along with other anti-cancer medicines.

    Who should not receive Doxorubicin?

    Do not receive Doxorubicin if:

    • you have had a recent heart attack or have severe heart problems
    • your blood cell counts (platelets, red blood cells, and white blood cells) are very low because of prior chemotherapy
    • you have a severe liver problem
    • you have had a serious allergic reaction to doxorubicin hydrochloride

    What should I tell my doctor before receiving Doxorubicin?

    Before you receive Doxorubicin, tell your doctor if you:

    • have heart problems including heart failure
    • are currently receiving radiation therapy or plan to receive radiation to the chest
    • have severe liver problems
    • have had an allergic reaction to doxorubicin
    • have any other medical conditions
    • are pregnant or plan to become pregnant. Doxorubicin can harm your unborn baby. Women who are able to become pregnant and men who take Doxorubicin should use effective birth control (contraception) during treatment and for 6 months after treatment. Talk to your doctor about birth control methods. If you or your partner becomes pregnant, tell your doctor right away.
    • are breastfeeding or plan to breast feed. Doxorubicin can pass into your breast milk and harm your baby. You and your doctor should decide if you will receive Doxorubicin or breastfeed. You should not do both.

    Tell your doctor about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Doxorubicin can interact with other medicines. Do not start any new medicine before you talk with the doctor that prescribed Doxorubicin.

    Know the medicines you take. Keep a list to show your doctor and pharmacist each time you get a new medicine.

    How will I receive Doxorubicin?

    • Doxorubicin will be given to you into your vein.

    What are the possible side effects of Doxorubicin?

    Doxorubicin may cause serious side effects, including:

    • See “What is the most important information I should know about Doxorubicin?”

    Doxorubicin may cause lower sperm counts and sperm problems in men.

    This could affect your ability to father a child and cause birth defects. Talk to your healthcare provider if this is a concern for you. Talk to your healthcare provider about family planning options that might be right for you.

    Irreversible amenorrhea or early menopause. Your periods (menstrual cycle) may completely stop when you receive Doxorubicin. Your periods may or may not return following treatment. Talk to your healthcare provider about family planning options that might be right for you.

    The most common side effects of Doxorubicin include:

    • Total hair loss (alopecia). Your hair may re-grow after your treatment
    • nausea
    • vomiting

    Other side effects:

    • Red colored urine. You may have red colored urine for 1 to 2 days after your infusion of Doxorubicin. This is normal. Tell your doctor if it does not stop in a few days, or if you see what looks like blood or blood clots in your urine.
    • Darkening of your nails or separation of your nails from your nail bed.
    • Easy bruising or bleeding.
    • Call your doctor if you have severe symptoms that prevent you from eating or drinking, such as:
      • nausea
      • vomiting
      • diarrhea
      • mouth sores

    Tell your doctor or nurse if you have any side effect that bothers you or that does not go away.

    These are not all of the possible side effects of Doxorubicin.

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

    General information about the safe and effective use of Doxorubicin.

    Medicines are sometimes prescribed for purposes other than those listed in a Patient Information leaflet.

    You can ask your pharmacist or doctor for information about Doxorubicin that is written for health professionals.

    For more information, call 1-877-845-0689.

    What are the ingredients of Doxorubicin?

    Active ingredient: doxorubicin hydrochloride

    Inactive ingredients for Doxorubicin Hydrochloride for Injection: Lactose Monohydrate.

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

    Manufactured by

    THYMOORGAN PHARMAZIE GmbH

    Schiffgraben 23, 38690 Goslar, Germany

    Distributed by

    Hikma Pharmaceuticals USA Inc.

    Berkeley Heights, NJ 07922

    Revised March 2021 

    127.207.045/00

  • 10 MG PACKAGE/LABEL PRINCIPAL DISPLAY PANEL

    NDC 0143-9092-01     Rx only
    DOXOrubicin
    HCl for Injection, USP
    10 mg per vial
    For Intravenous use ONLY
    LYOPHILIZED

    10 mg vial
  • 50 MG PACKAGE/LABEL PRINCIPAL DISPLAY PANEL

    NDC 0143-9093-01     Rx only
    DOXOrubicin
    HCl for Injection, USP
    50 mg per vial
    For Intravenous use ONLY
    LYOPHILIZED

    50 mg vial
  • INGREDIENTS AND APPEARANCE
    DOXORUBICIN HYDROCHLORIDE 
    doxorubicin hydrochloride injection, powder, lyophilized, for solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 0143-9092
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DOXORUBICIN HYDROCHLORIDE (UNII: 82F2G7BL4E) (DOXORUBICIN - UNII:80168379AG) DOXORUBICIN HYDROCHLORIDE2 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 0143-9092-011 in 1 BOX01/19/2018
    15 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA06292101/19/2018
    DOXORUBICIN HYDROCHLORIDE 
    doxorubicin hydrochloride injection, powder, lyophilized, for solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 0143-9093
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DOXORUBICIN HYDROCHLORIDE (UNII: 82F2G7BL4E) (DOXORUBICIN - UNII:80168379AG) DOXORUBICIN HYDROCHLORIDE2 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 0143-9093-011 in 1 BOX01/19/2018
    125 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA06292101/19/2018
    Labeler - Hikma Pharmaceuticals USA Inc. (001230762)
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