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    NDC 71205-0169-30 Gemfibrozil 600 mg/1 Details

    Gemfibrozil 600 mg/1

    Gemfibrozil is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Proficient Rx LP. The primary component is GEMFIBROZIL.

    Product Information

    NDC 71205-0169
    Product ID 71205-169_73ae4ea5-2353-487f-a6f1-04d0077fc551
    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, FILM COATED
    Route ORAL
    Active Ingredient Strength 600
    Active Ingredient Units mg/1
    Substance Name GEMFIBROZIL
    Labeler Name Proficient Rx LP
    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 ANDA202726
    Listing Certified Through 2024-12-31

    Package

    NDC 71205-0169-30 (71205016930)

    NDC Package Code 71205-169-30
    Billing NDC 71205016930
    Package 30 TABLET, FILM COATED in 1 BOTTLE (71205-169-30)
    Marketing Start Date 2018-12-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL e0cd766f-a1dd-440b-bfde-e2fb09f84a0e Details

    Revised: 11/2019