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    NDC 63629-1013-03 Famotidine 20 mg/1 Details

    Famotidine 20 mg/1

    Famotidine is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is FAMOTIDINE.

    Product Information

    NDC 63629-1013
    Product ID 63629-1013_9e2e08e6-20e8-4c9e-ab57-8400529b0408
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Famotidine
    Proprietary Name Suffix n/a
    Non-Proprietary Name Famotidine
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name FAMOTIDINE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA075805
    Listing Certified Through 2025-12-31

    Package

    NDC 63629-1013-03 (63629101303)

    NDC Package Code 63629-1013-3
    Billing NDC 63629101303
    Package 300 TABLET in 1 BOTTLE (63629-1013-3)
    Marketing Start Date 2012-04-10
    NDC Exclude Flag N
    Pricing Information N/A