Search by Drug Name or NDC

    NDC 42291-0936-90 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 AvKARE. The primary component is SUCRALFATE.

    Product Information

    NDC 42291-0936
    Product ID 42291-936_0909a2f4-ab61-2569-e063-6394a90acf6a
    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 AvKARE
    Pharmaceutical Class Aluminum Complex [EPC], Organometallic Compounds [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA215576
    Listing Certified Through 2024-12-31

    Package

    NDC 42291-0936-90 (42291093690)

    NDC Package Code 42291-936-90
    Billing NDC 42291093690
    Package 90 TABLET in 1 BOTTLE (42291-936-90)
    Marketing Start Date 2023-10-31
    NDC Exclude Flag N
    Pricing Information N/A