Search by Drug Name or NDC

    NDC 63187-0837-90 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 Proficient Rx LP. The primary component is PANTOPRAZOLE SODIUM.

    Product Information

    NDC 63187-0837
    Product ID 63187-837_06cc0229-6d8c-4b43-9936-391dd39975d5
    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
    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 Proficient Rx LP
    Pharmaceutical Class Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA205119
    Listing Certified Through 2024-12-31

    Package

    NDC 63187-0837-90 (63187083790)

    NDC Package Code 63187-837-90
    Billing NDC 63187083790
    Package 90 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-837-90)
    Marketing Start Date 2017-05-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL a7dc4321-331d-49af-976c-cfd69d0055d9 Details

    Revised: 5/2022