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    NDC 57896-0769-01 Famotidine 20 mg/1 Details

    Famotidine 20 mg/1

    Famotidine is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by GERI-CARE PHARMACEUTICAL CORP. The primary component is FAMOTIDINE.

    Product Information

    NDC 57896-0769
    Product ID 57896-769_d9e10fcb-ae1e-82a7-e053-2a95a90a43ce
    Associated GPIs
    GCN Sequence Number 011677
    GCN Sequence Number Description famotidine TABLET 20 MG ORAL
    HIC3 Z2D
    HIC3 Description HISTAMINE H2-RECEPTOR INHIBITORS
    GCN 46430
    HICL Sequence Number 004521
    HICL Sequence Number Description FAMOTIDINE
    Brand/Generic Generic
    Proprietary Name Famotidine
    Proprietary Name Suffix n/a
    Non-Proprietary Name Famotidine
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name FAMOTIDINE
    Labeler Name GERI-CARE PHARMACEUTICAL CORP
    Pharmaceutical Class Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090283
    Listing Certified Through 2023-12-31

    Package

    NDC 57896-0769-01 (57896076901)

    NDC Package Code 57896-769-01
    Billing NDC 57896076901
    Package 1 BOTTLE in 1 CARTON (57896-769-01) / 100 TABLET, FILM COATED in 1 BOTTLE
    Marketing Start Date 2022-02-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL cffaec6e-3455-84a6-e053-2a95a90a6a9f Details

    Revised: 3/2022