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    NDC 21130-0191-20 Famotidine 20 mg/1 Details

    Famotidine 20 mg/1

    Famotidine is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by SAFEWAY. The primary component is FAMOTIDINE.

    Product Information

    NDC 21130-0191
    Product ID 21130-191_0d1c33a5-8cd4-ec61-e063-6294a90a86e9
    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
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name FAMOTIDINE
    Labeler Name SAFEWAY
    Pharmaceutical Class Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA215822
    Listing Certified Through 2024-12-31

    Package

    NDC 21130-0191-20 (21130019120)

    NDC Package Code 21130-191-20
    Billing NDC 21130019120
    Package 200 TABLET in 1 BOTTLE (21130-191-20)
    Marketing Start Date 2023-06-30
    NDC Exclude Flag N
    Pricing Information N/A