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    NDC 11673-0158-04 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 11673-0158
    Product ID 11673-158_c2f6e780-a239-48e7-b825-508324a21fce
    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 (For Women)
    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 2023-12-31

    Package

    NDC 11673-0158-04 (11673015804)

    NDC Package Code 11673-158-04
    Billing NDC 11673015804
    Package 1 CAN in 1 CARTON (11673-158-04) / 60 g in 1 CAN
    Marketing Start Date 2022-08-16
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 3a6bef39-1d8e-4ce3-9484-becd294566da Details

    Revised: 10/2022