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    NDC 58914-0170-60 Carafate 1 g/10mL Details

    Carafate 1 g/10mL

    Carafate is a ORAL SUSPENSION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Allergan, Inc.. The primary component is SUCRALFATE.

    Product Information

    NDC 58914-0170
    Product ID 58914-170_cac080ef-887e-4b68-beb8-b0f90b86f458
    Associated GPIs 49300010001820
    GCN Sequence Number 016133
    GCN Sequence Number Description sucralfate ORAL SUSP 1 G/10 ML ORAL
    HIC3 D4E
    HIC3 Description ANTI-ULCER PREPARATIONS
    GCN 07651
    HICL Sequence Number 001186
    HICL Sequence Number Description SUCRALFATE
    Brand/Generic Brand
    Proprietary Name Carafate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Sucralfate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form SUSPENSION
    Route ORAL
    Active Ingredient Strength 1
    Active Ingredient Units g/10mL
    Substance Name SUCRALFATE
    Labeler Name Allergan, Inc.
    Pharmaceutical Class Aluminum Complex [EPC], Organometallic Compounds [CS]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA019183
    Listing Certified Through 2024-12-31

    Package

    NDC 58914-0170-60 (58914017060)

    NDC Package Code 58914-170-60
    Billing NDC 58914017060
    Package 6 CUP, UNIT-DOSE in 1 BOX (58914-170-60) / 295.7 mL in 1 CUP, UNIT-DOSE
    Marketing Start Date 1993-12-16
    NDC Exclude Flag N
    Pricing Information N/A