RABEPRAZOLE SODIUM DELAYED-RELEASE- rabeprazole sodium capsule, delayed release

rabeprazole sodium delayed-release by

Drug Labeling and Warnings

rabeprazole sodium delayed-release by is a Prescription medication manufactured, distributed, or labeled by Sarras Health, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • 1 INDICATIONS AND USAGE

    Rabeprazole sodium delayed-release capsules are indicated for treatment of Gastroesophageal Reflux Disease (GERD) in pediatric patients 1 to 11 years of age for up to 12 weeks.

  • 2 DOSAGE AND ADMINISTRATION

    2.1 Dosage Regimen

    Rabeprazole sodium delayed-release capsules are recommended for up to 12 weeks in pediatric patients 1 to 11 years of age and is dosed by body weight:

    • Less than 15 kg: 5 mg once daily with the option to increase to 10 mg once daily, if inadequate response.
    • 15 kg or more: 10 mg once daily.

    2.2 Administration Recommendations

    • Take the dose 30 minutes before a meal.
    • Do not swallow the capsule whole.
    • Open a capsule and sprinkle entire contents on a small amount of soft food (e.g., applesauce, fruit or vegetable based baby food, or yogurt) or empty contents into a small amount of liquid (e.g., infant formula, apple juice, or pediatric electrolyte solution). Food or liquid should be at or below room temperature.
    • Do not chew or crush the granules.
    • Take the entire dose within 15 minutes of preparation.
    • Do not store mixture for future use.
    • Take a missed dose as soon as possible. If it is almost time for the next dose, skip the missed dose and go back to the normal schedule. Do not take 2 doses at the same time.
  • 3 DOSAGE FORMS AND STRENGTHS

    Rabeprazole sodium delayed-release capsules (sprinkle) are provided as:

    • 10 mg: transparent yellow and opaque white No. 2 capsule imprinted with "↑" on the capsule cap and "ACX 10mg" on the capsule body.
  • 4 CONTRAINDICATIONS

    • Rabeprazole sodium delayed-release capsules are contraindicated in patients with known hypersensitivity to rabeprazole, substituted benzimidazoles, or to any component of the formulation. Hypersensitivity reactions may include anaphylaxis, anaphylactic shock, angioedema, bronchospasm, acute interstitial nephritis, and urticaria [see Adverse Reactions (6)].
    • PPIs, including rabeprazole sodium delayed-release capsules, are contraindicated with rilpivirine-containing products [see Drug Interactions (7)].
  • 5 WARNINGS AND PRECAUTIONS

    5.1 Presence of Gastric Malignancy

    In adults, symptomatic response to therapy with rabeprazole sodium delayed-release capsules does not preclude the presence of gastric malignancy. Consider additional follow-up and diagnostic testing in adult patients who have a suboptimal response or an early symptomatic relapse after completing treatment with a PPI. In older patients, also consider an endoscopy.

    5.2 Interaction with Warfarin

    Steady state interactions of rabeprazole and warfarin have not been adequately evaluated in patients. There have been reports of increased INR and prothrombin time in patients receiving a proton pump inhibitor and warfarin concomitantly. Increases in INR and prothrombin time may lead to abnormal bleeding and even death. Patients treated with rabeprazole sodium delayed-release capsules and warfarin concomitantly may need to be monitored for increases in INR and prothrombin time [see Drug Interactions (7)].

    5.3 Acute Interstitial Nephritis

    Acute interstitial nephritis has been observed in patients taking PPIs including rabeprazole sodium. Acute interstitial nephritis may occur at any point during PPI therapy and is generally attributed to an idiopathic hypersensitivity reaction. Discontinue rabeprazole sodium delayed-release capsules if acute interstitial nephritis develops [see Contraindications (4)].

    5.4 Clostridium difficile-Associated Diarrhea

    Published observational studies suggest that PPI therapy like rabeprazole sodium delayed-release capsules may be associated with an increased risk of Clostridium difficile-associated diarrhea, especially in hospitalized patients. This diagnosis should be considered for diarrhea that does not improve [see Adverse Reactions (6.2)].

    Patients should use the lowest dose and shortest duration of PPI therapy appropriate to the condition being treated.

    Clostridium difficile-associated diarrhea (CDAD) has been reported with use of nearly all antibacterial agents.

    5.5 Bone Fracture

    Several published observational studies in adults suggest that PPI therapy may be associated with an increased risk for osteoporosis-related fractures of the hip, wrist, or spine. The risk of fracture was increased in patients who received high-dose, defined as multiple daily doses, and long-term PPI therapy (a year or longer). Patients should use the lowest dose and shortest duration of PPI therapy appropriate to the condition being treated.

    Patients at risk for osteoporosis-related fractures should be managed according to established treatment guidelines [see Dosage and Administration (2), Adverse Reactions (6.2)].

    Rabeprazole sodium delayed-release capsules are indicated for short-term treatment up to 12 weeks. Treatment for longer than 12 weeks is not recommended.

    5.6 Cutaneous and Systemic Lupus Erythematosus

    Cutaneous lupus erythematosus (CLE) and systemic lupus erythematosus (SLE) have been reported in patients taking PPIs, including rabeprazole. These events have occurred as both new onset and an exacerbation of existing autoimmune disease. The majority of PPI-induced lupus erythematosus cases were CLE.

    The most common form of CLE reported in patients treated with PPIs was subacute CLE (SCLE) and occurred within weeks to years after continuous drug therapy in patients ranging from infants to the elderly. Generally, histological findings were observed without organ involvement.

    Systemic lupus erythematosus (SLE) is less commonly reported than CLE in patients receiving PPIs. PPI associated SLE is usually milder than non-drug induced SLE. Onset of SLE typically occurred within days to years after initiating treatment primarily in patients ranging from young adults to the elderly. The majority of patients presented with rash; however, arthralgia and cytopenia were also reported.

    Avoid administration of PPIs for longer than medically indicated. If signs or symptoms consistent with CLE or SLE are noted in patients receiving rabeprazole sodium delayed-release capsules, discontinue the drug and refer the patient to the appropriate specialist for evaluation. Most patients improve with discontinuation of the PPI alone in 4 to 12 weeks. Serological testing (e.g. ANA) may be positive and elevated serological test results may take longer to resolve than clinical manifestations.

    5.7 Cyanocobalamin (Vitamin B-12) Deficiency

    Daily treatment with any acid-suppressing medications over a long period of time (e.g., longer than 3 years) may lead to malabsorption of cyanocobalamin (vitamin B-12) caused by hypo- or achlorhydria. Rare reports of cyanocobalamin deficiency occurring with acid-suppressing therapy have been reported in the literature. This diagnosis should be considered if clinical symptoms consistent with cyanocobalamin deficiency are observed in patients treated with rabeprazole sodium delayed-release capsules.

    5.8 Hypomagnesemia

    Hypomagnesemia, symptomatic and asymptomatic, has been reported rarely in adult patients treated with PPIs for at least three months, in most cases after a year of therapy. Serious adverse events include tetany, arrhythmias, and seizures. In most patients, treatment of hypomagnesemia required magnesium replacement and discontinuation of the PPI.

    For patients expected to be on prolonged treatment or who take PPIs with medications such as digoxin or drugs that may cause hypomagnesemia (e.g., diuretics), healthcare professionals may consider monitoring magnesium levels prior to initiation of PPI treatment and periodically [see Adverse Reactions (6.2)].

    Rabeprazole sodium delayed-release capsules are indicated for short-term treatment of up to 12 weeks. Treatment for longer than 12 weeks is not recommended.

    5.9 Interaction with Methotrexate

    Literature suggests that concomitant use of PPIs with methotrexate (primarily at high dose; see methotrexate prescribing information) may elevate and prolong serum levels of methotrexate and/or its metabolite, possibly leading to methotrexate toxicities. In high-dose methotrexate administration, a temporary withdrawal of the PPI may be considered in some patients [see Drug Interactions (7)].

    5.10 Fundic Gland Polyps

    PPI use is associated with an increased risk of fundic gland polyps that increases with long-term use, especially beyond one year. Most PPI users who developed fundic gland polyps were asymptomatic and fundic gland polyps were identified incidentally on endoscopy. Use the shortest duration of PPI therapy appropriate to the condition being treated.

  • 6 ADVERSE REACTIONS

    The following serious adverse reactions are described below and elsewhere in labeling:

    6.1 Clinical Studies Experience

    Because clinical trials are conducted under 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.

    The efficacy of rabeprazole sodium delayed-release capsules was established in a two-part, randomized, multicenter, double-blind, parallel-group study of 127 pediatric patients 1 to 11 years of age with a history of at least one GERD symptom within the 3 months before screening and a positive esophagogastroduodenoscopy (EGD; Hetzel-Dent Endoscopic Classification System, Grade ≥1 and Histological Features of Reflux Esophagitis Scale, Grade >0). The two-part study consisted of a 12-week treatment period in patients with endoscopically-proven GERD followed by a 24-week, double-blinded extension study. Subjects had a mean age of 6 years (range: 1 to 11 years) and 44% (56/127) were female and 56% (71/127) were male. Of the 127 subjects enrolled, 78% (99/127) were white, 10% (13/127) were black, and 2% (3/127) were Asian.

    In the study, patients less than 15 kg body weight received either 5 mg or 10 mg rabeprazole sodium delayed-release capsules and patients 15 kg or greater body weight received 10 mg rabeprazole sodium delayed-release capsules. In this study, some patients were treated for 36 weeks. The most common adverse reactions leading to discontinuation were vomiting, abdominal pain, diarrhea, and nausea. The most common adverse reactions from the first 12 weeks of treatment are listed in Table 1.

    Table 1: Common Adverse Reactions* in Pediatric Study (Ages 1 To 11 Years First 12 Weeks of Treatment)
    Adverse ReactionPatients Less than 15 kgPatients 15 kg or greater
    5 mg
    (N=21)
    %    		10 mg
    (N=19)
    %    		10 mg
    (N=44)
    %
    * incidence of adverse reactions ≥9%
    Vomiting101114
    Abdominal Pain0016
    Diarrhea14219
    Headache009
    Nausea009

    The safety profile was similar for those patients who received treatment for up to 36 weeks.

    Adults and Adolescents Experience with Other Rabeprazole Formulations

    The data described below reflect exposure to rabeprazole sodium delayed-release tablets in 1064 adult patients exposed for up to 8 weeks. The studies were primarily placebo- and active-controlled trials in adult patients with Erosive or Ulcerative Gastroesophageal Reflux Disease (GERD), Duodenal Ulcers and Gastric Ulcers. The population had a mean age of 53 years (range 18-89 years) and had a ratio of approximately 60% male: 40% female. The racial distribution was 86% Caucasian, 8% African American, 2% Asian, and 5% other. Most patients received either 10 mg, 20 mg, or 40 mg per day of rabeprazole.

    An analysis of adverse reactions appearing in ≥2% of rabeprazole-treated patients (n=1064) and with a greater frequency than placebo (n=89) in controlled North American and European acute treatment trials, revealed the following adverse reactions: pain (3% vs. 1%), pharyngitis (3% vs. 2%), flatulence (3% vs. 1%), infection (2% vs. 1%), and constipation (2% vs. 1%).

    Other adverse reactions seen in controlled clinical trials, which do not meet the above criteria (≥2% of rabeprazole-treated patients and greater than placebo) and for which there is a possibility of a causal relationship to rabeprazole, include the following: headache, abdominal pain, diarrhea, dry mouth, dizziness, peripheral edema, hepatic enzyme increase, hepatitis, hepatic encephalopathy, myalgia, and arthralgia.

    In a multicenter, open-label study of adolescent patients 12 to 16 years of age with a clinical diagnosis of symptomatic GERD or endoscopically proven GERD, the adverse event profile was similar to that of adults. The adverse reactions reported without regard to relationship to rabeprazole that occurred in ≥2% of 111 patients were headache (9.9%), diarrhea (4.5%), nausea (4.5%), vomiting (3.6%), and abdominal pain (3.6%). The related reported adverse reactions that occurred in ≥2% of patients were headache (5.4%) and nausea (1.8%). There were no adverse reactions reported in this study that were not previously observed in adults.

    6.2 Postmarketing Experience

    The following adverse reactions have been identified during post approval use of rabeprazole sodium. 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.

    Blood and Lymphatic System Disorders: agranulocytosis, hemolytic anemia, leukopenia, pancytopenia, and thrombocytopenia
    Ear and Labyrinth Disorders: vertigo
    Eye Disorders: blurred vision
    Gastrointestinal Disorders: fundic gland polyps
    General Disorders and Administration Site Conditions: sudden death
    Hepatobiliary Disorders: jaundice
    Immune System Disorders: anaphylaxis, angioedema, systemic lupus erythematosus, Stevens-Johnson syndrome, toxic epidermal necrolysis (some fatal)
    Infections and Infestations: Clostridium difficile-associated diarrhea
    Investigations: Increases in prothrombin time/INR (in patients treated with concomitant warfarin), TSH elevations
    Metabolism and Nutrition Disorders: hyperammonemia, hypomagnesemia
    Musculoskeletal System Disorders: bone fracture, rhabdomyolysis
    Nervous System Disorders: coma
    Psychiatric Disorders: delirium, disorientation
    Renal and Urinary Disorders: interstitial nephritis
    Respiratory, Thoracic and Mediastinal Disorders: interstitial pneumonia
    Skin and Subcutaneous Tissue Disorders: severe dermatologic reactions, including bullous and other drug eruptions of the skin; cutaneous lupus erythematosus, erythema multiforme

  • 7 DRUG INTERACTIONS

    Table 2 includes clinically important drug interactions and interaction with diagnostics when administered concomitantly with rabeprazole sodium delayed-release capsules and instructions for preventing or managing them.

    Consult the labeling of concomitantly used drugs to obtain further information about interactions with PPIs.

    Table 2: Clinically Relevant Interactions Affecting Drugs Co-Administered with Rabeprazole Sodium Delayed-Release Capsules and Interactions with Diagnostics
    Antiretrovirals
    Clinical Impact:The effect of PPIs on antiretroviral drugs is variable. The clinical importance and the mechanisms behind these interactions are not always known.
    • Decreased exposure of some antiretroviral drugs (e.g., rilpivirine, atazanavir, nelfinavir) when used concomitantly with rabeprazole may reduce antiviral effect and promote the development of drug resistance
    • Increased exposure of other antiretroviral drugs (e.g., saquinavir) when used concomitantly with rabeprazole may increase toxicity.
    • There are other antiretroviral drugs which do not result in clinically relevant interactions with rabeprazole.
    Intervention:Rilpivirine-containing products: Concomitant use with rabeprazole sodium delayed-release capsules is contraindicated [see Contraindications (4)]. See prescribing information.
    Atazanavir: See prescribing information for atazanavir for dosing information.
    Nelfinavir: Avoid concomitant use with rabeprazole sodium delayed-release capsules. See prescribing information for nelfinavir.
    Saquinavir: See the prescribing information for saquinavir and monitor for potential saquinavir toxicities.
    Other antiretrovirals: See prescribing information.
    Warfarin
    Clinical Impact:Increased INR and prothrombin time in patients receiving PPIs, including rabeprazole, and warfarin concomitantly. Increases in INR and prothrombin time may lead to abnormal bleeding and even death [see Warnings and Precautions (5.2)].
    Intervention:Monitor INR and prothrombin time. Dose adjustment of warfarin may be needed to maintain target INR range. See prescribing information for warfarin.
    Methotrexate
    Clinical Impact:Concomitant use of rabeprazole with methotrexate (primarily at high dose) may elevate and prolong serum levels of methotrexate and/or its metabolite hydroxymethotrexate, possibly leading to methotrexate toxicities. No formal drug interaction studies of methotrexate with PPIs have been conducted [see Warnings and Precautions (5.9)].
    Intervention:A temporary withdrawal of rabeprazole sodium delayed-release capsules may be considered in some patients receiving high-dose methotrexate administration.
    Digoxin
    Clinical Impact:Potential for increased exposure of digoxin [see Clinical Pharmacology (12.3)].
    Intervention:Monitor digoxin concentrations. Dose adjustment of digoxin may be needed to maintain therapeutic drug concentrations. See prescribing information for digoxin.
    Drugs Dependent on Gastric pH for Absorption (e.g., iron salts, erlotinib, dasatinib, nilotinib, mycophenolate mofetil, ketoconazole, itraconazole)
    Clinical Impact:Rabeprazole can reduce the absorption of other drugs due to its effect on reducing intragastric acidity.
    Intervention:Mycophenolate mofetil (MMF): Co-administration of PPIs in healthy subjects and in transplant patients receiving MMF has been reported to reduce the exposure to the active metabolite, mycophenolic acid (MPA), possibly due to a decrease in MMF solubility at an increased gastric pH. The clinical relevance of reduced MPA exposure on organ rejection has not been established in transplant patients receiving rabeprazole sodium delayed-release capsules and MMF. Use rabeprazole sodium delayed-release capsules with caution in transplant patients receiving MMF.
    See the prescribing information for other drugs dependent on gastric pH for absorption.
    Tacrolimus
    Clinical Impact:Potentially increased exposure of tacrolimus, especially in transplant patients who are intermediate or poor metabolizers of CYP2C19.
    Intervention:Monitor tacrolimus whole blood trough concentrations. Dose adjustment of tacrolimus may be needed to maintain therapeutic drug concentrations. See prescribing information for tacrolimus.
    Interactions with Investigations of Neuroendocrine Tumors
    Clinical Impact:Serum chromogranin A (CgA) levels increase secondary to PPI-induced decreases in gastric acidity. The increased CgA level may cause false positive results in diagnostic investigations for neuroendocrine tumors.
    Intervention:Temporarily stop rabeprazole sodium delayed-release capsules treatment at least 14 days before assessing CgA levels and consider repeating the test if initial CgA levels are high. If serial tests are performed (e.g. for monitoring), the same commercial laboratory should be used for testing, as reference ranges between tests may vary.
    Interaction with Secretin Stimulation Test
    Clinical Impact:Hyper-response in gastrin secretion in adults in response to secretin stimulation test, falsely suggesting gastrinoma.
    Intervention:Temporarily stop treatment with rabeprazole sodium delayed-release capsules at least 14 days before assessing to allow gastrin levels to return to baseline.
    False Positive Urine Tests for THC
    Clinical Impact:There have been reports of false positive urine screening tests for tetrahydrocannabinol (THC) in patients receiving PPIs.
    Intervention:An alternative confirmatory method should be considered to verify positive results.

  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Risk Summary

    There are no available human data on rabeprazole sodium delayed-release capsules use in pregnant women to inform the drug associated risk. The background risk of major birth defects and miscarriage for the indicated populations are unknown. However, the background risk in the U.S. general population of major birth defects is 2-4% and of miscarriage is 15-20% of clinically recognized pregnancies. No evidence of adverse developmental effects were seen in animal reproduction studies with rabeprazole administered during organogenesis at 13 and 8 times the human area under the plasma concentration-time curve (AUC) at the recommended dose for GERD, in rats and rabbits, respectively [see Data].

    Changes in bone morphology were observed in offspring of rats treated with oral doses of a different PPI through most of pregnancy and lactation. When maternal administration was confined to gestation only, there were no effects on bone physeal morphology in the offspring at any age [see Data].

    Data

    Animal Data

    Embryo-fetal developmental studies have been performed in rats at intravenous doses of rabeprazole during organogenesis up to 50 mg/kg/day (plasma AUC of 11.8 µghr/mL, about 13 times the adult human exposure at the recommended oral dose for GERD) and rabbits at intravenous doses up to 30 mg/kg/day (plasma AUC of 7.3 µghr/mL, about 8 times the adult human exposure at the recommended oral dose for GERD: 20 mg of rabeprazole delayed-release tablets per day) and have revealed no evidence of harm to the fetus due to rabeprazole.

    Administration of rabeprazole to rats in late gestation and during lactation at an oral dose of 400 mg/kg/day (about 195 times the adult human oral dose based on mg/m2) resulted in decreases in body weight gain of the pups.

    A pre- and postnatal developmental toxicity study in rats with additional endpoints to evaluate bone development was performed with a different PPI at about 3.4 to 57 times an oral human dose on a body surface area basis. Decreased femur length, width and thickness of cortical bone, decreased thickness of the tibial growth plate, and minimal to mild bone marrow hypocellularity were noted at doses of this PPI equal to or greater than 3.4 times an oral human dose on a body surface area basis. Physeal dysplasia in the femur was also observed in offspring after in utero and lactational exposure to the PPI at doses equal to or greater than 33.6 times an oral human dose on a body surface area basis. Effects on maternal bone were observed in pregnant and lactating rats in a pre- and postnatal toxicity study when the PPI was administered at oral doses of 3.4 to 57 times an oral human dose on a body surface area basis. When rats were dosed from gestational day 7 through weaning on postnatal day 21, a statistically significant decrease in maternal femur weight of up to 14% (as compared to placebo treatment) was observed at doses equal to or greater than 33.6 times an oral human dose on a body surface area basis.

    A follow-up developmental toxicity study in rats with further time points to evaluate pup bone development from postnatal day 2 to adulthood was performed with a different PPI at oral doses of 280 mg/kg/day (about 68 times an oral human dose on a body surface area basis) where drug administration was from either gestational day 7 or gestational day 16 until parturition. When maternal administration was confined to gestation only, there were no effects on bone physeal morphology in the offspring at any age.

    8.2 Lactation

    Risk Summary

    Lactation studies have not been conducted to assess the presence of rabeprazole in human milk, the effects of rabeprazole on the breastfed infant, or the effects of rabeprazole on milk production. Rabeprazole is present in rat milk. The development and health benefits of breastfeeding should be considered along with the mother's clinical need for rabeprazole sodium delayed-release capsules and any potential adverse effects on the breastfed infant from rabeprazole sodium delayed-release capsules or from the underlying maternal condition.

    8.4 Pediatric Use

    GERD in Pediatric Patients 1 to 11 Years of Age

    The use of rabeprazole sodium delayed-release capsules for treatment of GERD in pediatric patients 1 to 11 years of age is supported by a randomized, multicenter, double-blind clinical trial which evaluated two dose levels of rabeprazole sodium delayed-release capsules in 127 pediatric patients with endoscopic and histologic evidence of GERD prior to study treatment. Dosing was determined by body weight: Patients weighing 6.0 to 14.9 kg received either 5 or 10 mg of rabeprazole sodium delayed-release capsules daily and those weighing 15.0 kg or more received 10 or 20 mg of rabeprazole sodium delayed-release capsules daily. After 12 weeks of rabeprazole treatment, 81% of patients demonstrated esophageal mucosal healing on endoscopic assessment. In patients who had esophageal mucosal healing at 12 weeks and elected to continue for 24 more weeks of rabeprazole, 90% retained esophageal mucosal healing at 36 weeks. No prespecified formal hypothesis testing for evaluation of efficacy was conducted. The absence of a placebo group does not allow assessment of sustained efficacy through 36 weeks. There were no adverse reactions reported in this study that were not previously observed in adolescents or adults.

    Symptomatic GERD in Infants 1 to 11 Months of Age

    The use of rabeprazole sodium delayed-release capsules is not recommended because studies conducted do not demonstrate efficacy for the treatment of GERD in pediatric patients younger than 1 year of age.

    In a randomized, multicenter, placebo-controlled withdrawal trial, infants 1 to 11 months of age with a clinical diagnosis of symptomatic GERD, or suspected or endoscopically proven GERD, were treated up to 8 weeks in two treatment periods. In the first treatment period (open-label), 344 infants received 10 mg of rabeprazole sodium delayed-release capsules for up to 3 weeks. Infants with clinical response were then eligible to enter the second treatment period, which was double-blind and randomized. Two hundred sixty-eight infants were randomized to receive either placebo or 5 mg or 10 mg rabeprazole sodium delayed-release capsules.

    This study did not demonstrate efficacy based on assessment of frequency of regurgitation and weight-for-age Z-score. Adverse reactions that occurred in ≥5% of patients in any treatment group and with a higher rate than placebo included pyrexia (7%) and increased serum gastrin levels (5%). There were no adverse reactions reported in this study that were not previously observed in adolescents and adults.

    Neonates <1 Month and Preterm Infants <44 Weeks Corrected Gestational Age

    The use of rabeprazole sodium delayed-release capsules is not recommended for the treatment of GERD, based on the risk of prolonged acid suppression and lack of demonstrated safety and effectiveness in neonates. Based on population pharmacokinetic analysis, the median (range) for the apparent clearance (CL/F) was 1.05 L/h (0.0543 to 3.44 L/h) in neonates and 4.46 L/h (0.822 to 12.4 L/h) in patients 1 to 11 months of age following once daily administration of oral rabeprazole sodium delayed-release capsules.

    Juvenile Animal Data

    Studies in juvenile and young adult rats and dogs were performed. In juvenile animal studies rabeprazole sodium was administered orally to rats for up to 5 weeks and to dogs for up to 13 weeks, each commencing on Day 7 post-partum and followed by a 13-week recovery period. Rats were dosed at 5, 25, or 150 mg/kg/day and dogs were dosed at 3, 10, or 30 mg/kg/day. The data from these studies were comparable to those reported for young adult animals. Pharmacologically mediated changes, including increased serum gastrin levels and stomach changes, were observed at all dose levels in both rats and dogs. These observations were reversible over the 13-week recovery periods. Although body weights and/or crown-rump lengths were minimally decreased during dosing, no effects on the development parameters were noted in either juvenile rats or dogs.

    When juvenile animals were treated for 28 days with a different PPI at doses equal to or greater than 34 times the daily oral human dose on a body surface area basis, overall growth was affected and treatment-related decreases in body weight (approximately 14%) and body weight gain, and decreases in femur weight and femur length were observed.

    8.5 Geriatric Use

    No studies with rabeprazole sodium delayed-release capsules have been conducted in geriatric patients. Rabeprazole sodium delayed-release capsules are not indicated for use in patients older than 11 years of age.

    8.6 Hepatic Impairment

    Administration of rabeprazole sodium delayed-release tablets to adult patients with mild to moderate hepatic impairment (Child-Pugh Class A and B, respectively) resulted in increased exposure and decreased elimination [see Clinical Pharmacology (12.3)]. No dosage adjustment of rabeprazole sodium delayed-release capsules is necessary in patients with mild to moderate hepatic impairment. There is no information in patients with severe hepatic impairment (Child-Pugh Class C). Avoid use of rabeprazole sodium delayed-release capsules in patients with severe hepatic impairment; however, if treatment is necessary, monitor patients for adverse reactions [see Warnings and Precautions (5), Adverse Reactions (6)].

  • 10 OVERDOSAGE

    Seven reports of accidental overdosage with rabeprazole have been received. The maximum reported overdose was 80 mg. There were no clinical signs or symptoms associated with any reported overdose. Patients with Zollinger-Ellison syndrome have been treated with up to 120 mg rabeprazole once daily. No specific antidote for rabeprazole is known. Rabeprazole is extensively protein bound and is not readily dialyzable.

    In the event of overdosage, treatment should be symptomatic and supportive.

    If over-exposure occurs, call your Poison Control Center at 1-800-222-1222 for current information on the management of poisoning or overdosage.

  • 11 DESCRIPTION

    The active ingredient in rabeprazole sodium delayed-release capsules is rabeprazole sodium, which is a proton pump inhibitor. It is a substituted benzimidazole known chemically as 2-[[[4-(3-methoxypropoxy)-3-methyl-2-pyridinyl]-methyl]sulfinyl]-1H–benzimidazole sodium salt. It has an empirical formula of C18H20N3NaO3S and a molecular weight of 381.42. Rabeprazole sodium is a white to slightly yellowish-white solid. It is very soluble in water and methanol, freely soluble in ethanol, chloroform, and ethyl acetate and insoluble in ether and n-hexane. The stability of rabeprazole sodium is a function of pH; it is rapidly degraded in acid media, and is more stable under alkaline conditions. The structural figure is:

    Figure 1

    Chemical Structure

    Rabeprazole sodium delayed-release capsules (sprinkle) are available for oral administration as 10 mg rabeprazole sodium delayed-release capsules containing enteric coated granules.

    Rabeprazole sodium delayed-release capsules contain granules of rabeprazole sodium in a hard hypromellose capsule. Inactive ingredients are colloidal silicon dioxide, diacetylated monoglycerides, ethylcellulose, hydroxypropyl cellulose, hypromellose phthalate, magnesium oxide, magnesium stearate, mannitol, talc, titanium dioxide, carrageenan, potassium chloride, FD&C Yellow, No. 6 (in the 10 mg capsule), and gray printing ink.

  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    Rabeprazole belongs to a class of antisecretory compounds (substituted benzimidazole proton-pump inhibitors) that do not exhibit anticholinergic or histamine H2-receptor antagonist properties, but suppress gastric acid secretion by inhibiting the gastric H+, K+ATPase at the secretory surface of the gastric parietal cell. Because this enzyme is regarded as the acid (proton) pump within the parietal cell, rabeprazole has been characterized as a gastric proton-pump inhibitor. Rabeprazole blocks the final step of gastric acid secretion.

    In gastric parietal cells, rabeprazole is protonated, accumulates, and is transformed to an active sulfenamide. When studied in vitro, rabeprazole is chemically activated at pH 1.2 with a half-life of 78 seconds. It inhibits acid transport in porcine gastric vesicles with a half-life of 90 seconds.

    12.3 Pharmacokinetics

    Absorption

    After oral administration to healthy adults of 10 mg rabeprazole sodium delayed-release capsules (delayed-release capsules opened and granules sprinkled on one tablespoon [15 mL] of applesauce) under fasting condition, median time (Tmax) to peak plasma concentrations (Cmax) of rabeprazole was 2.5 hours and ranged 1.0 to 6.5 hours. The plasma half-life of rabeprazole ranges from 1 to 2 hours.

    In healthy adults, a concomitant high fat meal delayed the absorption of rabeprazole from rabeprazole sodium delayed-release capsules (granules sprinkled on one tablespoon (15 mL) of applesauce) resulting in the median Tmax of 4.5 hours and decreased the Cmax and AUClast on average by 55% and 33%, respectively [see Dosage and Administration (2.2)].

    When 10 mg rabeprazole sodium delayed-release capsules (granules) administered under fasting conditions to healthy adults on one tablespoon (15 mL) of applesauce, one tablespoon (15 mL) of yogurt, or when mixed with a small amount (5 mL) of liquid infant formula; the type of soft food did not significantly affect Tmax, Cmax and AUC of rabeprazole.

    Distribution

    Rabeprazole is 96.3% bound to human plasma proteins.

    Elimination

    Metabolism: Rabeprazole is extensively metabolized. A significant portion of rabeprazole is metabolized via systemic nonenzymatic reduction to a thioether compound. Rabeprazole is also metabolized to sulphone and desmethyl compounds via cytochrome P450 in the liver. The thioether and sulphone are the primary metabolites measured in human plasma. These metabolites were not observed to have significant antisecretory activity. In vitro studies have demonstrated that rabeprazole is metabolized in the liver primarily by cytochromes P450 3A (CYP3A) to a sulphone metabolite and cytochrome P450 2C19 (CYP2C19) to desmethyl rabeprazole. CYP2C19 exhibits a known genetic polymorphism due to its deficiency in some sub-populations (e.g., 3 to 5% of Caucasians and 17 to 20% of Asians). Rabeprazole metabolism is slow in these sub-populations, therefore, they are referred to as poor metabolizers of the drug.

    Excretion: Following a single 20 mg oral dose of 14C-labeled rabeprazole, approximately 90% of the drug was eliminated in the urine, primarily as thioether carboxylic acid; its glucuronide, and mercapturic acid metabolites. The remainder of the dose was recovered in the feces. Total recovery of radioactivity was 99.8%. No unchanged rabeprazole was recovered in the urine or feces.

    Specific Populations

    Pediatric Patients: In patients with GERD 1 to 11 years of age, following once daily administration of rabeprazole sodium delayed-release capsules at doses from 0.14 to 1 mg/kg, the median time to peak plasma concentration ranged from 2 to 4 hours and the half-life was about 2.5 hours. No appreciable accumulation was noted following 5 days of dosing compared to exposure after a single dose.

    Based on population pharmacokinetic analysis, over the body weight range from 7 to 77 kg, the apparent rabeprazole clearance increased from 8.0 to 13.5 L/hr, an increase of 69%.

    The mean estimated total exposure i.e., AUC after a 10 mg dose of rabeprazole sodium delayed-release capsules in patients with GERD 1 to 11 years of age is comparable to AUC after 10 mg rabeprazole sodium delayed-release tablet in adults.

    Male and Female Patients and Racial or Ethnic Groups: In analyses of adult data adjusted for body mass and height, rabeprazole pharmacokinetics showed no clinically significant differences between male and female subjects. In studies that used different formulations of rabeprazole, AUC0-∞ values for healthy Japanese men were approximately 50 to 60% greater than values derived from pooled data from healthy men in the United States.

    Patients with Renal Impairment: In 10 adult patients with stable end-stage renal disease requiring maintenance hemodialysis (creatinine clearance ≤5 mL/min/1.73 m2), no clinically significant differences were observed in the pharmacokinetics of rabeprazole after administration of rabeprazole 20 mg delayed-release tablets when compared to 10 healthy adult subjects.

    Patients with Hepatic Impairment: In a single dose study of 10 adult patients with chronic mild to moderate hepatic impairment (Child-Pugh Class A and B, respectively) who were administered a 20 mg dose of rabeprazole sodium delayed-release tablets, AUC0-24 was approximately doubled, the elimination half-life was 2- to 3-fold higher, and total body clearance was decreased to less than half compared to values in healthy adult men.

    In a multiple dose study of 12 adult patients with mild to moderate hepatic impairment administered 20 mg rabeprazole sodium delayed-release tablets once daily for eight days, AUC0-∞ and Cmax values increased approximately 20% compared to values in healthy age- and gender-matched subjects. These increases were not statistically significant.

    No information exists on rabeprazole disposition in patients with severe hepatic impairment (Child-Pugh Class C) [see Use in Specific Populations (8.6)].

    Drug Interaction Studies

    Effects of Other Drugs on Rabeprazole

    Antacids: Co-administration of rabeprazole sodium delayed-release tablets and antacids produced no clinically relevant changes in plasma rabeprazole concentrations.

    Effects of Rabeprazole on Other Drugs

    Studies in healthy adult subjects have shown that rabeprazole does not have clinically significant interactions with other drugs metabolized by the CYP450 system, such as theophylline (CYP1A2) given as single oral doses, diazepam (CYP2C9 and CYP3A4) as a single intravenous dose, and phenytoin (CYP2C9 and CYP2C19) given as a single intravenous dose (with supplemental oral dosing). Steady state interactions of rabeprazole and other drugs metabolized by this enzyme system have not been studied in patients.

    Clopidogrel: Clopidogrel is metabolized to its active metabolite in part by CYP2C19. A study of healthy adult subjects including CYP2C19 extensive and intermediate metabolizers receiving once daily administration of clopidogrel 75 mg concomitantly with placebo or with 20 mg rabeprazole sodium delayed-release tablets (n=36), for 7 days was conducted. The mean AUC of the active metabolite of clopidogrel was reduced by approximately 12% (mean AUC ratio was 88%, with 90% CI of 81.7 to 95.5%) when rabeprazole sodium delayed-release tablets was co-administered compared to administration of clopidogrel with placebo [see Drug Interactions (7)].

    Digoxin: In healthy adult subjects (n=16), co-administration of 20 mg rabeprazole sodium delayed-release tablets with 2.5 mg once daily doses of digoxin at steady state resulted in approximately 29% and 19% increase in mean Cmax and AUC(0-24) of digoxin [see Drug Interactions (7)].

    Ketoconazole: In healthy adult subjects (n=19), co-administration of 20 mg rabeprazole sodium delayed-release tablets at steady state with a single 400 mg oral dose ketoconazole resulted in approximately an average of 31% reduction in both Cmax and AUC(0-inf) of ketoconazole [see Drug Interactions (7)].

    Cyclosporine: In vitro incubations employing human liver microsomes indicated that rabeprazole inhibited cyclosporine metabolism with an IC50 of 62 micromolar, a concentration that is over 50 times higher than the Cmax in healthy volunteers following 14 days of dosing with 20 mg of rabeprazole sodium delayed-release tablets. This degree of inhibition is similar to that by omeprazole at equivalent concentrations.

    12.5 Pharmacogenomics

    In a clinical study in Japan evaluating rabeprazole sodium delayed-release tablets in Japanese adult patients categorized by CYP2C19 genotype (n=6 per genotype category), gastric acid suppression was higher in poor metabolizers as compared to extensive metabolizers. The clinical relevance of this is not known. This could be due to higher rabeprazole plasma levels in poor metabolizers. Whether or not interactions of rabeprazole sodium with other drugs metabolized by CYP2C19 would be different between extensive metabolizers and poor metabolizers has not been studied.

  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    In an 88/104-week carcinogenicity study in CD-1 mice, rabeprazole at oral doses up to 100 mg/kg/day did not produce any increased tumor occurrence. The highest tested dose produced a systemic exposure to rabeprazole (AUC) of 1.40 µghr/mL which is 1.6 times the adult human exposure (plasma AUC0-∞ = 0.88 µghr/mL) at the recommended dose for GERD (20 mg of rabeprazole sodium delayed-release tablets per day). In a 28-week carcinogenicity study in p53+/- transgenic mice, rabeprazole at oral doses of 20, 60, and 200 mg/kg/day did not cause an increase in the incidence rates of tumors but produced gastric mucosal hyperplasia at all doses. The systemic exposure to rabeprazole at 200 mg/kg/day is about 17 to 24 times the adult human exposure at the recommended dose for GERD (20 mg of rabeprazole sodium delayed-release tablets per day). In a 104-week carcinogenicity study in Sprague-Dawley rats, males were treated with oral doses of 5, 15, 30, and 60 mg/kg/day and females with 5, 15, 30, 60, and 120 mg/kg/day. Rabeprazole produced gastric enterochromaffin-like (ECL) cell hyperplasia in male and female rats and ECL cell carcinoid tumors in female rats at all doses including the lowest tested dose. The lowest dose (5 mg/kg/day) produced a systemic exposure to rabeprazole (AUC) of about 0.1 µghr/mL which is about 0.1 times the adult human exposure at the recommended dose for GERD (20 mg of rabeprazole sodium delayed-release tablets per day). In male rats, no treatment-related tumors were observed at doses up to 60 mg/kg/day producing a rabeprazole plasma exposure (AUC) of about 0.2 µghr/mL (0.2 times the adult human exposure at the recommended dose for GERD).

    Rabeprazole was positive in the Ames test, the Chinese hamster ovary cell (CHO/HGPRT) forward gene mutation test, and the mouse lymphoma cell (L5178Y/TK+/–) forward gene mutation test. Its demethylated-metabolite was also positive in the Ames test. Rabeprazole was negative in the in vitro Chinese hamster lung cell chromosome aberration test, the in vivo mouse micronucleus test, and the in vivo and ex vivo rat hepatocyte unscheduled DNA synthesis (UDS) tests.

    Rabeprazole at intravenous doses up to 30 mg/kg/day (plasma AUC of 8.8 µghr/mL, about 10 times the adult human exposure at the recommended dose for GERD) was found to have no effect on fertility and reproductive performance of male and female rats. The recommended dose for GERD in adults is 20 mg per day (rabeprazole sodium delayed-release tablets).

  • 14 CLINICAL STUDIES

    The use of rabeprazole sodium delayed-release capsules in pediatric patients 1 to 11 years of age is supported by a two-part, multicenter, randomized, double-blind, parallel 2 dose arms clinical trial which was conducted in 127 pediatric patients with endoscopic and histologic evidence of GERD prior to study treatment.

    Part 1 of the trial was 12 weeks in duration. Patients were randomized to one of two rabeprazole dose levels based on body weight. Patients weighing 6 to 14.9 kg received either 5 or 10 mg rabeprazole sodium delayed-release capsules, and those with body weight ≥15 kg received 10 mg rabeprazole sodium delayed-release capsules. Part 2 was a 24-week double-blinded extension of Part 1 (on same dose assigned in Part 1). Endoscopic evaluations were performed at 12 weeks (Part 1) and 36 weeks (Part 2) to assess esophageal healing. No prespecified formal hypothesis testing was conducted.

    For Part 1, rates of endoscopic healing were calculated and are shown in Table 3.

    Table 3: Short-Term (12-Week) Healing Rates In 1 To 11 Year Old Children (Part 1)
    Endoscopic
    Classification of GERD
    At Baseline    		Healing Rate at 12 weeks
    Body Weight Less than 15 kgBody Weight 15 kg or Greater
    5 mg dose10 mg dose10 mg dose
    a Hetzel-Dent score ≥2
    b Hetzel-Dent score = 1
    Erosivea88% (7/8)83% (5/6)71% (12/17)
    Non-erosiveb78% (7/9)100% (10/10)81% (17/21)

    Of the 87 patients with healing in Part 1, 64 patients were enrolled into Part 2. The absence of a placebo group does not allow assessment of sustained efficacy through 36 weeks. Of the 52 patients with available data, healing was observed in 47 (90%) patients at 36 weeks.

    The recommended dosage of rabeprazole sodium delayed-release capsules is 5 mg once daily for 12 weeks in patients less than 15 kg with the option to increase to 10 mg once daily if there is an inadequate response. In patients 15 kg or greater, the recommended dosage is 10 mg once daily for 12 weeks.

  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    Rabeprazole sodium delayed-release capsules (10 mg) (sprinkle) are supplied as transparent yellow and opaque white capsules containing enteric coated granules. Identification and strength (ACX 10mg) are imprinted on the body of the capsule. An arrow (↑) imprint on the capsule cap indicates direction for opening a capsule.

    Bottles of 30 (NDC: 72834-210-30)

    Store at 25°C (77°F); excursions permitted to 15-30°C (59-86°F) [see USP Controlled Room Temperature]. Protect from moisture.

  • 17 PATIENT COUNSELING INFORMATION

    Advise the patient or caregiver to read the FDA-approved patient labeling (Medication Guide).

    Acute Interstitial Nephritis

    Advise the patient or caregiver to call the patient’s healthcare provider immediately if they experience signs and/or symptoms associated with acute interstitial nephritis [see Warnings and Precautions (5.3)].

    Clostridium difficile-Associated Diarrhea

    Advise the patient or caregiver to immediately call the patient’s healthcare provider if they experience diarrhea that does not improve [see Warnings and Precautions (5.4)].

    Bone Fracture

    Advise the patient or caregiver to report any fractures, especially of the hip, wrist or spine, to the patient’s healthcare provider [see Warnings and Precautions (5.5)].

    Cutaneous and Systemic Lupus Erythematosus

    Advise the patient or caregiver to immediately call the patient’s healthcare provider for any new or worsening of symptoms associated with cutaneous or systemic lupus erythematosus [see Warnings and Precautions (5.6)]

    Cyanocobalamin (Vitamin B-12) Deficiency

    Advise the patient or caregiver to report any clinical symptoms that may be associated with cyanocobalamin deficiency to the patient’s healthcare provider if they have been receiving rabeprazole sodium delayed-release capsules for longer than 3 years [see Warnings and Precautions (5.7)].

    Hypomagnesemia

    Advise the patient or caregiver to report any clinical symptoms that may be associated with hypomagnesemia to the patient’s healthcare provider, if they have been receiving rabeprazole sodium delayed-release capsules for at least 3 months [see Warnings and Precautions (5.8)].

    Drug Interactions

    Advise the patient or caregiver to report to the patient’s healthcare provider if they are taking rilpilvirine-containing products [see Contraindications (4)], warfarin or high-dose methotrexate [see Warnings and Precautions (5.2, 5.9)].

    Administration

    • Take the dose 30 minutes before a meal.
    • Do not swallow the capsule whole.
    • Open the rabeprazole sodium delayed-release capsule and sprinkle the granule contents on a small amount of soft food (e.g., applesauce, fruit or vegetable based baby food, or yogurt) or empty contents into a small amount of liquid (e.g., infant formula, apple juice, or pediatric electrolyte solution). Food or liquid should be at or below room temperature.
    • Do not chew or crush the granules.
    • Take the entire dose within 15 minutes of preparation.
    • Do not store mixture for future use.
    • Take a missed dose as soon as possible. If it is almost time for the next dose, skip the missed dose and go back to the normal schedule. Do not take 2 doses at the same time.
  • SPL UNCLASSIFIED SECTION

    Distributed and Marketed by Sarras Health, LLC, Athens, GA 30601

  • MEDICATION GUIDE

    MEDICATION GUIDE
    Rabeprazole Sodium Delayed Release Capsules (Sprinkle)

    What is the most important information I should know about rabeprazole sodium delayed-release capsules?
    Your child should take rabeprazole sodium delayed-release capsules exactly as prescribed, at the lowest dose possible and for the shortest time needed.
    Rabeprazole sodium delayed-release capsules may help your child's acid-related symptoms, but your child could still have serious stomach problems. Talk with your child's doctor.
    Rabeprazole sodium delayed-release capsules can cause serious side effects, including:

    • A type of kidney problem (acute interstitial nephritis). Some people who take proton pump inhibitor (PPI) medicines, including rabeprazole sodium delayed-release capsules, may develop a kidney problem called acute interstitial nephritis that can happen at any time during treatment with rabeprazole sodium delayed-release capsules. Call your child’s doctor right away if your child has a decrease in the amount that they urinate or if they have blood in their urine.
    • Diarrhea caused by an infection (Clostridium difficile) in your child’s intestines. Call your child’s doctor right away if your child has watery stools or stomach pain that does not go away. Your child may or may not have a fever.
    • Bone fractures (hip, wrist or spine). Bone fractures in the hip, wrist or spine may happen in people who take multiple daily doses of PPI medicines and for a long period of time (a year or longer). Tell your child’s doctor if your child has a bone fracture, especially in the hip, wrist or spine.
    • Certain types of lupus erythematosus. Lupus erythematosus is an autoimmune disorder (the body’s immune cells attack other cells or organs in the body). Some people who take PPI medicines, including rabeprazole sodium delayed-release capsules, may develop certain types of lupus erythematosus or have worsening of the lupus they already have. Call your child’s doctor right away if they have new or worsening joint pain or a rash on their cheeks or arms that gets worse in the sun.

    Talk to your child’s doctor about your child’s risk of serious side effects.
    Rabeprazole sodium delayed-release capsules can have other serious side effects. See "What are the possible side effects of rabeprazole sodium delayed-release capsules?"

    What are rabeprazole sodium delayed-release capsules?
    Rabeprazole sodium delayed-release capsules are a prescription medicine called a proton pump inhibitor (PPI). Rabeprazole sodium delayed-release capsules reduce the amount of acid in the stomach.
    Rabeprazole sodium delayed-release capsules are used in children 1 year to 11 years of age to treat Gastroesophageal Reflux Disease (GERD) for up to 12 weeks.
    Rabeprazole sodium delayed-release capsules are not effective in treating GERD in children under 1 year of age.
    Rabeprazole sodium delayed-release capsules should not be used to treat GERD in babies younger than 1 month of age.

    Your child should not take rabeprazole sodium delayed-release capsules if they are:

    • allergic to rabeprazole, any other PPI medicine, or any of the ingredients in rabeprazole sodium delayed-release capsules. See the end of this Medication Guide for a complete list of ingredients.
    • taking a medicine that contains rilpivirine (EDURANT, COMPLERA, ODEFSEY) used to treat HIV-1 (Human Immunodeficiency Virus).

    Before your child takes rabeprazole sodium delayed-release capsules, tell your child’s doctor about all of your child’s medical conditions, including if they:

    • have low magnesium levels in their blood.
    • have liver problems.
    • are pregnant or plan to become pregnant. It is not known if rabeprazole sodium delayed-release capsules can harm an unborn baby.
    • are breastfeeding or plan to breastfeed. It is not known if rabeprazole sodium delayed-release capsules passes into breast milk. Talk to your child’s doctor about the best way to feed her baby if she takes rabeprazole sodium delayed-release capsules.

    Tell your child’s doctor about all the medicines your child takes, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Especially tell your child’s doctor if your child takes warfarin (COUMADIN, JANTOVEN) or methotrexate (Otrexup, Rasuvo,Trexall, Xatmep).

    How should my child take rabeprazole sodium delayed-release capsules?

    • Your child should take rabeprazole sodium delayed-release capsules exactly as prescribed. Your child’s doctor will prescribe the dose that is right for your child.
    • Your child should take rabeprazole sodium delayed-release capsules 1 time each day.
    • Your child should take rabeprazole sodium delayed-release capsules 30 minutes before a meal.
    • Your child should not swallow the rabeprazole sodium delayed-release capsule whole.
    • Prepare and give a dose of rabeprazole sodium delayed-release capsules to your child as follows:
      • Open the rabeprazole sodium delayed-release capsule in the direction that the arrow (↑) on the capsule is pointing. Sprinkle all of the capsule contents onto a small amount of soft food such as applesauce, fruit or vegetable based baby food, or yogurt. You may also empty all of the capsule contents into a small amount of infant formula, apple juice, or a pediatric electrolyte solution. The food or liquid that you use should be at or below room temperature.
      • Your child should swallow the entire mixture. They should not chew or crush the granules.
      • Your child should take the entire dose within 15 minutes of preparing it. Do not save it for use later.
    • If your child misses a dose of rabeprazole sodium delayed-release capsules, they should take it as soon as possible. If it is almost time for their next dose, they should not take the missed dose. Your child should take their next dose at their regular time. They should not take 2 doses at the same time.
    • If your child takes too much rabeprazole sodium delayed-release capsules, call your child’s doctor or your poison control center at 1-800-222-1222 right away, or go to the nearest emergency room.

    What are the possible side effects of rabeprazole sodium delayed-release capsules?
    Rabeprazole sodium delayed-release capsules can cause serious side effects, including:

    • See "What is the most important information I should know about rabeprazole sodium delayed-release capsules?"
    • Interaction with warfarin. Taking warfarin with a PPI medicine may lead to an increased risk of bleeding and death. If your child takes warfarin, their doctor may check their blood to see if they have an increased risk of bleeding. If your child takes warfarin during treatment with rabeprazole sodium delayed-release capsules, tell their doctor right away if they have any signs or symptoms of bleeding, including:
      • pain, swelling or discomfort
      • headaches, dizziness, or weakness
      • unusual bruising (bruises that happen without known cause or that grow in size)
      • nosebleeds
      • bleeding gums
      • bleeding from cuts takes a long time to stop
      • menstrual bleeding that is heavier than normal
      • pink or brown urine
      • red or black stools
      • coughing up blood
      • vomiting blood or vomit that looks like coffee grounds
    • Low vitamin B-12 levels in the body can happen in people who have taken rabeprazole sodium delayed-release capsules for a long time (more than 3 years). Tell your child’s doctor if your child has symptoms of low vitamin B-12 levels, including shortness of breath, lightheadedness, irregular heartbeat, muscle weakness, pale skin, feeling tired, mood changes, and tingling or numbness in the arms and legs.
    • Low magnesium levels in the body can happen in people who have taken rabeprazole sodium delayed-release capsules for at least 3 months. Tell your child’s doctor if your child has symptoms of low magnesium levels, including seizures, dizziness, irregular heartbeat, jitteriness, muscle aches or weakness, and spasms of hands, feet or voice.
    • Stomach growths (fundic gland polyps). People who take PPI medicines for a long time have an increased risk of developing a certain type of stomach growths called fundic gland polyps, especially after taking PPI medicines for more than 1 year.

    The most common side effects of rabeprazole sodium delayed-release capsules include: vomiting, stomach-area (abdomen) pain, diarrhea, headache, and nausea.
    These are not all of the possible side effects of rabeprazole sodium delayed-release capsules. Call your child’s doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

    How should I store rabeprazole sodium delayed-release capsules?
    Store rabeprazole sodium delayed-release capsules in a dry place at room temperature between 68°F to 77°F (20°C to 25°C).
    Keep rabeprazole sodium delayed-release capsules and all medicines out of the reach of children.

    General Information about the safe and effective use of rabeprazole sodium delayed-release capsules.
    Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use rabeprazole sodium delayed-release capsules for a condition for which it was not prescribed. Do not give rabeprazole sodium delayed-release capsules to other people, even if they have the same symptoms that you have. It may harm them.
    You can ask your child's doctor or pharmacist for information about rabeprazole sodium delayed-release capsules that is written for health professionals.

    What are the ingredients in rabeprazole sodium delayed-release capsules?
    Active ingredient: rabeprazole sodium
    Inactive ingredients: colloidal silicon dioxide, diacetylated monoglycerides, ethylcellulose, hydroxypropyl cellulose, hypromellose phthalate, magnesium oxide, magnesium stearate, mannitol, talc, titanium dioxide, carrageenan, potassium chloride, FD&C Yellow, No. 6 (in the 10 mg capsule), and gray printing ink.

    Distributed and Marketed by Sarras Health, LLC
    Athens, GA 30601

    This Medication Guide has been approved by the U.S. Food and Drug Administration.

    Revised: April 2019

  • PRINCIPAL DISPLAY PANEL - 10 mg Bottle Label

    NDC: 72834-210-30

    Rx only

    Rabeprazole
    Sodium Delayed
    Release Capsules
    (Sprinkle)

    sarras health

    10 mg

    30 capsules

    10 mg Bottle Label

  • INGREDIENTS AND APPEARANCE
    RABEPRAZOLE SODIUM DELAYED-RELEASE 
    rabeprazole sodium capsule, delayed release
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 72834-210
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RABEPRAZOLE SODIUM (UNII: 3L36P16U4R) (RABEPRAZOLE - UNII:32828355LL) RABEPRAZOLE SODIUM10 mg
    Inactive Ingredients
    Ingredient NameStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    DIACETYLATED MONOGLYCERIDES (UNII: 5Z17386USF)  
    ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)  
    HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P)  
    HYPROMELLOSE PHTHALATE (24% PHTHALATE, 55 CST) (UNII: 87Y6436BKR)  
    MAGNESIUM OXIDE (UNII: 3A3U0GI71G)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MANNITOL (UNII: 3OWL53L36A)  
    TALC (UNII: 7SEV7J4R1U)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    CARRAGEENAN (UNII: 5C69YCD2YJ)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    Product Characteristics
    ColorYELLOW (transparent) , WHITE (opaque) Scoreno score
    ShapeCAPSULE (Oval) Size10mm
    FlavorImprint Code ACX;10mg
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 72834-210-3030 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/27/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDA authorized genericNDA20473606/27/2019
    Labeler - Sarras Health, LLC (116763528)
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