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    NDC 30142-0557-55 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 Kroger Company. The primary component is OMEPRAZOLE.

    Product Information

    NDC 30142-0557
    Product ID 30142-557_4e390c9f-df66-4288-a43a-078cb675782a
    Associated GPIs
    GCN Sequence Number 054334
    GCN Sequence Number Description omeprazole TABLET DR 20 MG ORAL
    HIC3 D4J
    HIC3 Description PROTON-PUMP INHIBITORS
    GCN 22228
    HICL Sequence Number 004673
    HICL Sequence Number Description OMEPRAZOLE
    Brand/Generic Generic
    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 Kroger Company
    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 30142-0557-55 (30142055755)

    NDC Package Code 30142-557-55
    Billing NDC 30142055755
    Package 3 CARTON in 1 CARTON (30142-557-55) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
    Marketing Start Date 2008-02-25
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 015b1c8f-9d5b-4afc-a55c-1a731b5fc72a Details

    Revised: 7/2022