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    NDC 70934-0280-30 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 Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is AMIODARONE HYDROCHLORIDE.

    Product Information

    NDC 70934-0280
    Product ID 70934-280_f057a3e9-ea33-5eae-e053-2a95a90ac0bc
    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 Denton Pharma, Inc. DBA Northwind Pharmaceuticals
    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 ANDA204742
    Listing Certified Through n/a

    Package

    NDC 70934-0280-30 (70934028030)

    NDC Package Code 70934-280-30
    Billing NDC 70934028030
    Package 30 TABLET in 1 BOTTLE, PLASTIC (70934-280-30)
    Marketing Start Date 2019-02-13
    NDC Exclude Flag N
    Pricing Information N/A
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