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    NDC 51655-0797-52 Pantoprazole Sodium 40 mg/1 Details

    Pantoprazole Sodium 40 mg/1

    Pantoprazole Sodium is a ORAL TABLET, DELAYED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Northwind Pharmaceuticals, LLC. The primary component is PANTOPRAZOLE SODIUM.

    Product Information

    NDC 51655-0797
    Product ID 51655-797_082791c9-6ae3-1451-e063-6294a90a6195
    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 Pantoprazole Sodium
    Proprietary Name Suffix n/a
    Non-Proprietary Name Pantoprazole Sodium
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, DELAYED RELEASE
    Route ORAL
    Active Ingredient Strength 40
    Active Ingredient Units mg/1
    Substance Name PANTOPRAZOLE SODIUM
    Labeler Name Northwind Pharmaceuticals, LLC
    Pharmaceutical Class Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202038
    Listing Certified Through 2024-12-31

    Package

    NDC 51655-0797-52 (51655079752)

    NDC Package Code 51655-797-52
    Billing NDC 51655079752
    Package 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-797-52)
    Marketing Start Date 2022-02-21
    NDC Exclude Flag N
    Pricing Information N/A