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    NDC 69842-0087-80 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 CVS Pharmacy, Inc.. The primary component is FAMOTIDINE.

    Product Information

    NDC 69842-0087
    Product ID 69842-087_fe9a2cc4-b5bc-4941-a4a1-040f4c5393bd
    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 OTC DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name FAMOTIDINE
    Labeler Name CVS Pharmacy, Inc.
    Pharmaceutical Class Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA206531
    Listing Certified Through 2025-12-31

    Package

    NDC 69842-0087-80 (69842008780)

    NDC Package Code 69842-087-80
    Billing NDC 69842008780
    Package 2 BOTTLE in 1 CARTON (69842-087-80) / 100 TABLET, FILM COATED in 1 BOTTLE
    Marketing Start Date 2021-01-25
    NDC Exclude Flag N
    Pricing Information N/A