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    NDC 72189-0234-90 SUCRALFATE 1 g/1 Details

    SUCRALFATE 1 g/1

    SUCRALFATE is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by DIRECT RX. The primary component is SUCRALFATE.

    Product Information

    NDC 72189-0234
    Product ID 72189-234_d1243811-c096-53f9-e053-2995a90abd74
    Associated GPIs 49300010000305
    GCN Sequence Number 002766
    GCN Sequence Number Description sucralfate TABLET 1 G ORAL
    HIC3 D4E
    HIC3 Description ANTI-ULCER PREPARATIONS
    GCN 08200
    HICL Sequence Number 001186
    HICL Sequence Number Description SUCRALFATE
    Brand/Generic Generic
    Proprietary Name SUCRALFATE
    Proprietary Name Suffix n/a
    Non-Proprietary Name SUCRALFATE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 1
    Active Ingredient Units g/1
    Substance Name SUCRALFATE
    Labeler Name DIRECT RX
    Pharmaceutical Class Aluminum Complex [EPC], Organometallic Compounds [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA070848
    Listing Certified Through 2024-12-31

    Package

    NDC 72189-0234-90 (72189023490)

    NDC Package Code 72189-234-90
    Billing NDC 72189023490
    Package 90 TABLET in 1 BOTTLE (72189-234-90)
    Marketing Start Date 2021-06-18
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL c50b5044-31ed-672a-e053-2995a90a49fc Details

    Revised: 11/2021