Search by Drug Name or NDC

    NDC 31722-0526-10 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 Camber Pharmaceuticals, Inc.. The primary component is FINASTERIDE.

    Product Information

    NDC 31722-0526
    Product ID 31722-526_0ebbabf3-0681-484d-ab8d-58e670d80a0d
    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 Camber Pharmaceuticals, Inc.
    Pharmaceutical Class 5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090060
    Listing Certified Through 2024-12-31

    Package

    NDC 31722-0526-10 (31722052610)

    NDC Package Code 31722-526-10
    Billing NDC 31722052610
    Package 1000 TABLET, FILM COATED in 1 BOTTLE (31722-526-10)
    Marketing Start Date 2013-07-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 00e934bb-c15b-490a-a852-839689a1231a Details

    Revised: 7/2017