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    NDC 50090-5796-00 Fenofibrate 145 mg/1 Details

    Fenofibrate 145 mg/1

    Fenofibrate is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is FENOFIBRATE.

    Product Information

    NDC 50090-5796
    Product ID 50090-5796_78a1916f-fe3e-47c5-85f2-77a9a1ea9920
    Associated GPIs
    GCN Sequence Number 061200
    GCN Sequence Number Description fenofibrate nanocrystallized TABLET 145 MG ORAL
    HIC3 M4E
    HIC3 Description LIPOTROPICS
    GCN 97003
    HICL Sequence Number 033904
    HICL Sequence Number Description FENOFIBRATE NANOCRYSTALLIZED
    Brand/Generic Generic
    Proprietary Name Fenofibrate
    Proprietary Name Suffix n/a
    Non-Proprietary Name fenofibrate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 145
    Active Ingredient Units mg/1
    Substance Name FENOFIBRATE
    Labeler Name A-S Medication Solutions
    Pharmaceutical Class Peroxisome Proliferator Receptor alpha Agonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA200884
    Listing Certified Through 2024-12-31

    Package

    NDC 50090-5796-00 (50090579600)

    NDC Package Code 50090-5796-0
    Billing NDC 50090579600
    Package 90 TABLET, FILM COATED in 1 BOTTLE (50090-5796-0)
    Marketing Start Date 2021-10-13
    NDC Exclude Flag N
    Pricing Information N/A