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    NDC 70934-0255-90 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 Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is GEMFIBROZIL.

    Product Information

    NDC 70934-0255
    Product ID 70934-255_d5f6a05f-3876-822a-e053-2995a90a19bd
    Associated GPIs 39200030000310
    GCN Sequence Number 006416
    GCN Sequence Number Description gemfibrozil TABLET 600 MG ORAL
    HIC3 M4E
    HIC3 Description LIPOTROPICS
    GCN 25540
    HICL Sequence Number 002766
    HICL Sequence Number Description GEMFIBROZIL
    Brand/Generic Generic
    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 Denton Pharma, Inc. DBA Northwind Pharmaceuticals
    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 ANDA077836
    Listing Certified Through n/a

    Package

    NDC 70934-0255-90 (70934025590)

    NDC Package Code 70934-255-90
    Billing NDC 70934025590
    Package 90 TABLET in 1 BOTTLE, PLASTIC (70934-255-90)
    Marketing Start Date 2019-01-22
    NDC Exclude Flag N
    Pricing Information N/A