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    NDC 68788-7853-09 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 Preferred Pharmaceuticals Inc.. The primary component is FAMOTIDINE.

    Product Information

    NDC 68788-7853
    Product ID 68788-7853_c9b914a2-0c99-4bcb-9416-a34e7c44703b
    Associated GPIs 49200030000320
    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 Preferred Pharmaceuticals Inc.
    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 2024-12-31

    Package

    NDC 68788-7853-09 (68788785309)

    NDC Package Code 68788-7853-9
    Billing NDC 68788785309
    Package 90 TABLET in 1 BOTTLE (68788-7853-9)
    Marketing Start Date 2021-01-29
    NDC Exclude Flag N
    Pricing Information N/A