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    NDC 68788-7922-09 Famotidine 40 mg/1 Details

    Famotidine 40 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 68788-7922
    Product ID 68788-7922_c2bfe453-e0a6-4f85-9145-2f8e2e3ca733
    Associated GPIs 49200030000340
    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 40
    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 68788-7922-09 (68788792209)

    NDC Package Code 68788-7922-9
    Billing NDC 68788792209
    Package 90 TABLET in 1 BOTTLE (68788-7922-9)
    Marketing Start Date 2021-06-14
    NDC Exclude Flag N
    Pricing Information N/A