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    NDC 51672-4057-00 Amiodarone Hydrochloride 400 mg/1 Details

    Amiodarone Hydrochloride 400 mg/1

    Amiodarone Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Taro Pharmaceuticals U.S.A., Inc.. The primary component is AMIODARONE HYDROCHLORIDE.

    Product Information

    NDC 51672-4057
    Product ID 51672-4057_74e1d323-cd6f-41c3-9b5c-0f40e7acf27c
    Associated GPIs 35400005000320
    GCN Sequence Number 047421
    GCN Sequence Number Description amiodarone HCl TABLET 400 MG ORAL
    HIC3 A2A
    HIC3 Description ANTIARRHYTHMICS
    GCN 12465
    HICL Sequence Number 000083
    HICL Sequence Number Description AMIODARONE HCL
    Brand/Generic Generic
    Proprietary Name Amiodarone Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Amiodarone Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 400
    Active Ingredient Units mg/1
    Substance Name AMIODARONE HYDROCHLORIDE
    Labeler Name Taro Pharmaceuticals U.S.A., Inc.
    Pharmaceutical Class Antiarrhythmic [EPC], Cytochrome P450 1A2 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076362
    Listing Certified Through 2024-12-31

    Package

    NDC 51672-4057-00 (51672405700)

    NDC Package Code 51672-4057-0
    Billing NDC 51672405700
    Package 10 BLISTER PACK in 1 CARTON (51672-4057-0) / 10 TABLET in 1 BLISTER PACK
    Marketing Start Date 2002-11-29
    NDC Exclude Flag N
    Pricing Information N/A