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    NDC 51662-1205-01 AMIODARONE HYDROCHLORIDE 50 mg/mL Details

    AMIODARONE HYDROCHLORIDE 50 mg/mL

    AMIODARONE HYDROCHLORIDE is a INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by HF Acquisition Co LLC, DBA HealthFirst. The primary component is AMIODARONE HYDROCHLORIDE.

    Product Information

    NDC 51662-1205
    Product ID 51662-1205_0ef250d9-ba34-8a3e-e063-6394a90acd14
    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 INJECTION, SOLUTION
    Route INTRAVENOUS
    Active Ingredient Strength 50
    Active Ingredient Units mg/mL
    Substance Name AMIODARONE HYDROCHLORIDE
    Labeler Name HF Acquisition Co LLC, DBA HealthFirst
    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 ANDA077234
    Listing Certified Through 2025-12-31

    Package

    NDC 51662-1205-01 (51662120501)

    NDC Package Code 51662-1205-1
    Billing NDC 51662120501
    Package 3 mL in 1 VIAL, SINGLE-DOSE (51662-1205-1)
    Marketing Start Date 2018-09-19
    NDC Exclude Flag N
    Pricing Information N/A