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    NDC 17856-0306-01 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 ATLANTIC BIOLOGICALS CORP.. The primary component is SUCRALFATE.

    Product Information

    NDC 17856-0306
    Product ID 17856-0306_e7155d7d-45e1-4b47-82c9-5036eb8d2394
    Associated GPIs
    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 ATLANTIC BIOLOGICALS CORP.
    Pharmaceutical Class Aluminum Complex [EPC], Organometallic Compounds [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA211884
    Listing Certified Through 2024-12-31

    Package

    NDC 17856-0306-01 (17856030601)

    NDC Package Code 17856-0306-1
    Billing NDC 17856030601
    Package 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0306-1) / 10 mL in 1 CUP, UNIT-DOSE (17856-0306-2)
    Marketing Start Date 2023-08-10
    NDC Exclude Flag N
    Pricing Information N/A