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    NDC 51672-4056-06 Amiodarone Hydrochloride 300 mg/1 Details

    Amiodarone Hydrochloride 300 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 51672-4056
    Product ID 51672-4056_74e1d323-cd6f-41c3-9b5c-0f40e7acf27c
    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 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 300
    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 51672-4056-06 (51672405606)

    NDC Package Code 51672-4056-6
    Billing NDC 51672405606
    Package 30 TABLET in 1 BOTTLE (51672-4056-6)
    Marketing Start Date 2003-12-02
    NDC Exclude Flag N
    Pricing Information N/A
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