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    NDC 41250-0349-55 Omeprazole 20 mg/1 Details

    Omeprazole 20 mg/1

    Omeprazole is a ORAL TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by Meijer Distribution Inc. The primary component is OMEPRAZOLE.

    Product Information

    NDC 41250-0349
    Product ID 41250-349_196181dd-ca33-481c-87c0-d662346b7660
    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, ORALLY DISINTEGRATING, DELAYED RELEASE
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name OMEPRAZOLE
    Labeler Name Meijer Distribution Inc
    Pharmaceutical Class Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA209400
    Listing Certified Through 2024-12-31

    Package

    NDC 41250-0349-55 (41250034955)

    NDC Package Code 41250-349-55
    Billing NDC 41250034955
    Package 3 CARTON in 1 CARTON (41250-349-55) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK
    Marketing Start Date 2018-03-13
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL d54e1097-bd56-4371-8e59-8ceab1a5e824 Details

    Revised: 4/2019