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    NDC 50090-5327-00 FENOFIBRATE 48 mg/1 Details

    FENOFIBRATE 48 mg/1

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

    Product Information

    NDC 50090-5327
    Product ID 50090-5327_107dcbf9-9c02-41fe-859d-e9b418b62d3c
    Associated GPIs
    GCN Sequence Number 061199
    GCN Sequence Number Description fenofibrate nanocrystallized TABLET 48 MG ORAL
    HIC3 M4E
    HIC3 Description LIPOTROPICS
    GCN 97002
    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
    Route ORAL
    Active Ingredient Strength 48
    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 ANDA208709
    Listing Certified Through 2024-12-31

    Package

    NDC 50090-5327-00 (50090532700)

    NDC Package Code 50090-5327-0
    Billing NDC 50090532700
    Package 90 TABLET in 1 BOTTLE (50090-5327-0)
    Marketing Start Date 2020-10-30
    NDC Exclude Flag N
    Pricing Information N/A