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    NDC 67877-0455-05 Finasteride 1 mg/1 Details

    Finasteride 1 mg/1

    Finasteride is a ORAL TABLET, COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Ascend Laboratories, LLC. The primary component is FINASTERIDE.

    Product Information

    NDC 67877-0455
    Product ID 67877-455_1c62ec5c-cd32-4478-92e6-03769fe541cc
    Associated GPIs 90736030000310
    GCN Sequence Number 037050
    GCN Sequence Number Description finasteride TABLET 1 MG ORAL
    HIC3 L1C
    HIC3 Description HYPERTRICHOTIC AGENTS, SYSTEMIC/INCL. COMBINATIONS
    GCN 29248
    HICL Sequence Number 006421
    HICL Sequence Number Description FINASTERIDE
    Brand/Generic Generic
    Proprietary Name Finasteride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Finasteride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, COATED
    Route ORAL
    Active Ingredient Strength 1
    Active Ingredient Units mg/1
    Substance Name FINASTERIDE
    Labeler Name Ascend Laboratories, LLC
    Pharmaceutical Class 5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA207750
    Listing Certified Through 2024-12-31

    Package

    NDC 67877-0455-05 (67877045505)

    NDC Package Code 67877-455-05
    Billing NDC 67877045505
    Package 500 TABLET, COATED in 1 BOTTLE (67877-455-05)
    Marketing Start Date 2017-01-06
    NDC Exclude Flag N
    Pricing Information N/A