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    NDC 43598-0469-52 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 43598-0469
    Product ID 43598-469_3fb729ea-a04a-bfdd-d564-7045771e1247
    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 43598-0469-52 (43598046952)

    NDC Package Code 43598-469-52
    Billing NDC 43598046952
    Package 1 BOTTLE in 1 CARTON (43598-469-52) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
    Marketing Start Date 2020-11-15
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 94e0d10a-4c72-4e58-abf7-cc00f7b90b23 Details

    Revised: 7/2020