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    NDC 63629-7300-05 Amiodarone hydrochloride 200 mg/1 Details

    Amiodarone hydrochloride 200 mg/1

    Amiodarone hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is AMIODARONE HYDROCHLORIDE.

    Product Information

    NDC 63629-7300
    Product ID 63629-7300_ded19b13-99a4-47c6-86b6-5ca93aa47527
    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 200
    Active Ingredient Units mg/1
    Substance Name AMIODARONE HYDROCHLORIDE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Antiarrhythmic [EPC], Cytochrome P450 1A2 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA079029
    Listing Certified Through 2023-12-31

    Package

    NDC 63629-7300-05 (63629730005)

    NDC Package Code 63629-7300-5
    Billing NDC 63629730005
    Package 10 TABLET in 1 BOTTLE (63629-7300-5)
    Marketing Start Date 2021-12-22
    NDC Exclude Flag N
    Pricing Information N/A