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    NDC 68788-7964-06 GEMFIBROZIL 600 mg/1 Details

    GEMFIBROZIL 600 mg/1

    GEMFIBROZIL is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. The primary component is GEMFIBROZIL.

    Product Information

    NDC 68788-7964
    Product ID 68788-7964_d58aa377-a202-474b-b64d-44509b805e44
    Associated GPIs 39200030000310
    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 GEMFIBROZIL
    Proprietary Name Suffix n/a
    Non-Proprietary Name Gemfibrozil
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 600
    Active Ingredient Units mg/1
    Substance Name GEMFIBROZIL
    Labeler Name Preferred Pharmaceuticals, Inc.
    Pharmaceutical Class PPAR alpha [CS], Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator-activated Receptor alpha Agonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA214603
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7964-06 (68788796406)

    NDC Package Code 68788-7964-6
    Billing NDC 68788796406
    Package 60 TABLET in 1 BOTTLE (68788-7964-6)
    Marketing Start Date 2021-07-20
    NDC Exclude Flag N
    Pricing Information N/A