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    NDC 59779-0580-01 Omeprazole 20 mg/1 Details

    Omeprazole 20 mg/1

    Omeprazole is a ORAL TABLET, DELAYED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by CVS Pharmacy. The primary component is OMEPRAZOLE.

    Product Information

    NDC 59779-0580
    Product ID 59779-580_6e980235-4aa7-4876-b079-f700dc31c7e1
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Omeprazole
    Proprietary Name Suffix n/a
    Non-Proprietary Name Omeprazole
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, DELAYED RELEASE
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name OMEPRAZOLE
    Labeler Name CVS Pharmacy
    Pharmaceutical Class Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA022032
    Listing Certified Through 2024-12-31

    Package

    NDC 59779-0580-01 (59779058001)

    NDC Package Code 59779-580-01
    Billing NDC 59779058001
    Package 1 BOTTLE in 1 CARTON (59779-580-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
    Marketing Start Date 2015-03-31
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 19b5b960-cc4d-42d0-8c8a-04a355a4db92 Details

    Revised: 7/2022