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    NDC 60505-0222-02 Sotalol Hydrochloride 80 mg/1 Details

    Sotalol Hydrochloride 80 mg/1

    Sotalol Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Apotex Corp.. The primary component is SOTALOL HYDROCHLORIDE.

    Product Information

    NDC 60505-0222
    Product ID 60505-0222_1fc1a2cf-5e7e-1cde-6dea-b0deb10cfac7
    Associated GPIs 33100045120310
    GCN Sequence Number 017196
    GCN Sequence Number Description sotalol HCl TABLET 80 MG ORAL
    HIC3 J7C
    HIC3 Description BETA-ADRENERGIC BLOCKING AGENTS
    GCN 39512
    HICL Sequence Number 004791
    HICL Sequence Number Description SOTALOL HCL
    Brand/Generic Generic
    Proprietary Name Sotalol Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Sotalol Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 80
    Active Ingredient Units mg/1
    Substance Name SOTALOL HYDROCHLORIDE
    Labeler Name Apotex Corp.
    Pharmaceutical Class Adrenergic beta-Antagonists [MoA], Antiarrhythmic [EPC], Cardiac Rhythm Alteration [PE]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076214
    Listing Certified Through 2024-12-31

    Package

    NDC 60505-0222-02 (60505022202)

    NDC Package Code 60505-0222-2
    Billing NDC 60505022202
    Package 1000 TABLET in 1 BOTTLE, PLASTIC (60505-0222-2)
    Marketing Start Date 2003-09-09
    NDC Exclude Flag N
    Pricing Information N/A