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    NDC 63187-0863-20 Finasteride 1 mg/1 Details

    Finasteride 1 mg/1

    Finasteride 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 FINASTERIDE.

    Product Information

    NDC 63187-0863
    Product ID 63187-863_fdd2ba1f-49ae-46cb-8c9c-47d2b0d659ab
    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, FILM COATED
    Route ORAL
    Active Ingredient Strength 1
    Active Ingredient Units mg/1
    Substance Name FINASTERIDE
    Labeler Name Proficient Rx LP
    Pharmaceutical Class 5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA091643
    Listing Certified Through 2024-12-31

    Package

    NDC 63187-0863-20 (63187086320)

    NDC Package Code 63187-863-20
    Billing NDC 63187086320
    Package 20 TABLET, FILM COATED in 1 BOTTLE (63187-863-20)
    Marketing Start Date 2022-02-11
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 870ab7fe-fff9-4348-b900-213c1cf05f8e Details

    Revised: 6/2022