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    NDC 75907-0119-27 Esomeprazole Magnesium 20 mg/1 Details

    Esomeprazole Magnesium 20 mg/1

    Esomeprazole Magnesium is a ORAL TABLET, DELAYED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by Dr. Reddys Laboratories Inc. The primary component is ESOMEPRAZOLE MAGNESIUM.

    Product Information

    NDC 75907-0119
    Product ID 75907-119_a40c48e8-93c4-8b65-6b4d-a6d236e39c38
    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 Esomeprazole Magnesium
    Proprietary Name Suffix n/a
    Non-Proprietary Name Esomeprazole Magnesium
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, DELAYED RELEASE
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name ESOMEPRAZOLE MAGNESIUM
    Labeler Name Dr. Reddys Laboratories Inc
    Pharmaceutical Class Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA211571
    Listing Certified Through 2024-12-31

    Package

    NDC 75907-0119-27 (75907011927)

    NDC Package Code 75907-119-27
    Billing NDC 75907011927
    Package 2 BOTTLE in 1 CARTON (75907-119-27) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
    Marketing Start Date 2023-12-30
    NDC Exclude Flag N
    Pricing Information N/A