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    NDC 72882-0094-73 Minoxidil 50 mg/mL Details

    Minoxidil 50 mg/mL

    Minoxidil is a TOPICAL SOLUTION in the HUMAN OTC DRUG category. It is labeled and distributed by Mens LLC. The primary component is MINOXIDIL.

    Product Information

    NDC 72882-0094
    Product ID 72882-094_04c4dc43-730e-447e-b96c-25481971723b
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Minoxidil
    Proprietary Name Suffix Extra Strength for Men
    Non-Proprietary Name Minoxidil
    Product Type HUMAN OTC DRUG
    Dosage Form SOLUTION
    Route TOPICAL
    Active Ingredient Strength 50
    Active Ingredient Units mg/mL
    Substance Name MINOXIDIL
    Labeler Name Mens LLC
    Pharmaceutical Class Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA075518
    Listing Certified Through 2024-12-31

    Package

    NDC 72882-0094-73 (72882009473)

    NDC Package Code 72882-094-73
    Billing NDC 72882009473
    Package 1 BOTTLE, DROPPER in 1 CARTON (72882-094-73) / 60 mL in 1 BOTTLE, DROPPER
    Marketing Start Date 2020-05-21
    NDC Exclude Flag N
    Pricing Information N/A