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    NDC 65862-0559-99 Pantoprazole Sodium 20 mg/1 Details

    Pantoprazole Sodium 20 mg/1

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

    Product Information

    NDC 65862-0559
    Product ID 65862-559_4f55b3b5-70cb-4168-bf64-3db08a685e68
    Associated GPIs 49270070100610
    GCN Sequence Number 039545
    GCN Sequence Number Description pantoprazole sodium TABLET DR 20 MG ORAL
    HIC3 D4J
    HIC3 Description PROTON-PUMP INHIBITORS
    GCN 95976
    HICL Sequence Number 022008
    HICL Sequence Number Description PANTOPRAZOLE SODIUM
    Brand/Generic Generic
    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 20
    Active Ingredient Units mg/1
    Substance Name PANTOPRAZOLE SODIUM
    Labeler Name Aurobindo Pharma Limited
    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 65862-0559-99 (65862055999)

    NDC Package Code 65862-559-99
    Billing NDC 65862055999
    Package 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-559-99)
    Marketing Start Date 2012-09-28
    NDC Exclude Flag N
    Pricing Information N/A