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    NDC 51672-4060-01 Amcinonide 1 mg/g Details

    Amcinonide 1 mg/g

    Amcinonide is a TOPICAL OINTMENT in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Taro Pharmaceuticals U.S.A., Inc.. The primary component is AMCINONIDE.

    Product Information

    NDC 51672-4060
    Product ID 51672-4060_0e7f65fb-5a8e-087b-e063-6294a90a9b38
    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 Amcinonide
    Proprietary Name Suffix n/a
    Non-Proprietary Name Amcinonide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form OINTMENT
    Route TOPICAL
    Active Ingredient Strength 1
    Active Ingredient Units mg/g
    Substance Name AMCINONIDE
    Labeler Name Taro Pharmaceuticals U.S.A., Inc.
    Pharmaceutical Class Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076367
    Listing Certified Through 2025-12-31

    Package

    NDC 51672-4060-01 (51672406001)

    NDC Package Code 51672-4060-1
    Billing NDC 51672406001
    Package 1 TUBE in 1 CARTON (51672-4060-1) / 15 g in 1 TUBE
    Marketing Start Date 2003-03-19
    NDC Exclude Flag N
    Pricing Information N/A
    << 51672-4057-06 51672-4060-02 >>

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