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    NDC 70518-3246-00 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 REMEDYREPACK INC.. The primary component is AMIODARONE HYDROCHLORIDE.

    Product Information

    NDC 70518-3246
    Product ID 70518-3246_f7936176-e699-88b0-e053-6394a90a1489
    Associated GPIs 35400005000305
    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 REMEDYREPACK INC.
    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 ANDA213446
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-3246-00 (70518324600)

    NDC Package Code 70518-3246-0
    Billing NDC 70518324600
    Package 30 TABLET in 1 BLISTER PACK (70518-3246-0)
    Marketing Start Date 2021-10-15
    NDC Exclude Flag N
    Pricing Information N/A