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    NDC 69339-0148-17 Sucralfate 1 g/10mL Details

    Sucralfate 1 g/10mL

    Sucralfate is a ORAL SUSPENSION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Natco Pharma USA LLC. The primary component is SUCRALFATE.

    Product Information

    NDC 69339-0148
    Product ID 69339-148_4f2d0850-0a70-4509-aed1-8844b5f095c6
    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 Generic
    Proprietary Name Sucralfate
    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 Natco Pharma USA LLC
    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 69339-0148-17 (69339014817)

    NDC Package Code 69339-148-17
    Billing NDC 69339014817
    Package 4 TRAY in 1 CASE (69339-148-17) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (69339-148-01)
    Marketing Start Date 2021-01-27
    NDC Exclude Flag N
    Pricing Information N/A