Search by Drug Name or NDC

    NDC 71335-1125-02 Sotalol Hydrochloride 120 mg/1 Details

    Sotalol Hydrochloride 120 mg/1

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

    Product Information

    NDC 71335-1125
    Product ID 71335-1125_0365b32c-9701-4e6c-8457-8468c1ffd27c
    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 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 120
    Active Ingredient Units mg/1
    Substance Name SOTALOL HYDROCHLORIDE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Adrenergic beta-Antagonists [MoA], Antiarrhythmic [EPC], Cardiac Rhythm Alteration [PE]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076140
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-1125-02 (71335112502)

    NDC Package Code 71335-1125-2
    Billing NDC 71335112502
    Package 30 TABLET in 1 BOTTLE (71335-1125-2)
    Marketing Start Date 2018-12-28
    NDC Exclude Flag N
    Pricing Information N/A