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    NDC 72578-0081-06 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 Viona Pharmaceuticals Inc. The primary component is SUCRALFATE.

    Product Information

    NDC 72578-0081
    Product ID 72578-081_50be7e37-3381-49ff-afe2-ca6a50245bf8
    Associated GPIs
    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 Viona Pharmaceuticals Inc
    Pharmaceutical Class Aluminum Complex [EPC], Organometallic Compounds [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA215705
    Listing Certified Through 2024-12-31

    Package

    NDC 72578-0081-06 (72578008106)

    NDC Package Code 72578-081-06
    Billing NDC 72578008106
    Package 30 TABLET in 1 BOTTLE (72578-081-06)
    Marketing Start Date 2023-05-20
    NDC Exclude Flag N
    Pricing Information N/A