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    NDC 11673-0157-09 Minoxidil 50 mg/g Details

    Minoxidil 50 mg/g

    Minoxidil is a TOPICAL AEROSOL, FOAM in the HUMAN OTC DRUG category. It is labeled and distributed by TARGET Corporation. The primary component is MINOXIDIL.

    Product Information

    NDC 11673-0157
    Product ID 11673-157_f75739eb-2e71-45f8-9cc8-023400615f57
    Associated GPIs 43997002520910
    GCN Sequence Number 016414
    GCN Sequence Number Description guaifenesin/dextromethorphan SYRUP 100-10MG/5 ORAL
    HIC3 B3T
    HIC3 Description NON-OPIOID ANTITUSSIVE AND EXPECTORANT COMBINATION
    GCN 53495
    HICL Sequence Number 000223
    HICL Sequence Number Description GUAIFENESIN/DEXTROMETHORPHAN HBR
    Brand/Generic Generic
    Proprietary Name Minoxidil
    Proprietary Name Suffix (For Men)
    Non-Proprietary Name Minoxidil
    Product Type HUMAN OTC DRUG
    Dosage Form AEROSOL, FOAM
    Route TOPICAL
    Active Ingredient Strength 50
    Active Ingredient Units mg/g
    Substance Name MINOXIDIL
    Labeler Name TARGET Corporation
    Pharmaceutical Class Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA209074
    Listing Certified Through 2024-12-31

    Package

    NDC 11673-0157-09 (11673015709)

    NDC Package Code 11673-157-09
    Billing NDC 11673015709
    Package 3 CAN in 1 CARTON (11673-157-09) / 60 g in 1 CAN (11673-157-01)
    Marketing Start Date 2022-08-16
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 5505e1b2-8c9b-457c-8291-cb8a9c1f6b10 Details

    Revised: 10/2022