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    NDC 59640-0023-71 acid reducer 20 mg/1 Details

    acid reducer 20 mg/1

    acid reducer is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by H E B. The primary component is FAMOTIDINE.

    Product Information

    NDC 59640-0023
    Product ID 59640-023_71f282a6-8ecc-41d4-9cda-7d70950669fe
    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 acid reducer
    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 H E B
    Pharmaceutical Class Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077351
    Listing Certified Through 2024-12-31

    Package

    NDC 59640-0023-71 (59640002371)

    NDC Package Code 59640-023-71
    Billing NDC 59640002371
    Package 1 BOTTLE in 1 CARTON (59640-023-71) / 50 TABLET, FILM COATED in 1 BOTTLE
    Marketing Start Date 2022-12-19
    NDC Exclude Flag N
    Pricing Information N/A
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