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    NDC 59779-0732-01 Omeprazole and Sodium Bicarbonate 20; 1100 mg/1; mg/1 Details

    Omeprazole and Sodium Bicarbonate 20; 1100 mg/1; mg/1

    Omeprazole and Sodium Bicarbonate is a ORAL CAPSULE, GELATIN COATED in the HUMAN OTC DRUG category. It is labeled and distributed by CVS Pharmacy. The primary component is OMEPRAZOLE; SODIUM BICARBONATE.

    Product Information

    NDC 59779-0732
    Product ID 59779-732_9a11d3ba-dd24-4026-b65b-0eecac3eb3aa
    Associated GPIs 49996002600120
    GCN Sequence Number 060471
    GCN Sequence Number Description omeprazole/sodium bicarbonate CAPSULE 20MG-1.1G ORAL
    HIC3 D4J
    HIC3 Description PROTON-PUMP INHIBITORS
    GCN 26632
    HICL Sequence Number 033512
    HICL Sequence Number Description OMEPRAZOLE/SODIUM BICARBONATE
    Brand/Generic Generic
    Proprietary Name Omeprazole and Sodium Bicarbonate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Omeprazole, sodium bicarbonate
    Product Type HUMAN OTC DRUG
    Dosage Form CAPSULE, GELATIN COATED
    Route ORAL
    Active Ingredient Strength 20; 1100
    Active Ingredient Units mg/1; mg/1
    Substance Name OMEPRAZOLE; SODIUM BICARBONATE
    Labeler Name CVS Pharmacy
    Pharmaceutical Class Cytochrome P450 2C19 Inhibitors [MoA], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA201361
    Listing Certified Through 2024-12-31

    Package

    NDC 59779-0732-01 (59779073201)

    NDC Package Code 59779-732-01
    Billing NDC 59779073201
    Package 1 BOTTLE in 1 CARTON (59779-732-01) / 14 CAPSULE, GELATIN COATED in 1 BOTTLE
    Marketing Start Date 2016-07-15
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 186732a3-13b9-4ea2-ba54-424f63298a2e Details

    Revised: 10/2020