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    NDC 63629-2680-03 Benazepril Hydrochloride and Hydrochlorothiazide 20; 12.5 mg/1; mg/1 Details

    Benazepril Hydrochloride and Hydrochlorothiazide 20; 12.5 mg/1; mg/1

    Benazepril Hydrochloride and Hydrochlorothiazide is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE.

    Product Information

    NDC 63629-2680
    Product ID 63629-2680_dc00e0fc-3f68-4608-7dc1-2ca800827a6d
    Associated GPIs 36991802150330
    GCN Sequence Number 021725
    GCN Sequence Number Description benazepril/hydrochlorothiazide TABLET 20-12.5 MG ORAL
    HIC3 A4J
    HIC3 Description ACE INHIBITOR-THIAZIDE OR THIAZIDE-LIKE DIURETIC
    GCN 33193
    HICL Sequence Number 008962
    HICL Sequence Number Description BENAZEPRIL HCL/HYDROCHLOROTHIAZIDE
    Brand/Generic Generic
    Proprietary Name Benazepril Hydrochloride and Hydrochlorothiazide
    Proprietary Name Suffix n/a
    Non-Proprietary Name Benazepril Hydrochloride and Hydrochlorothiazide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 20; 12.5
    Active Ingredient Units mg/1; mg/1
    Substance Name BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076631
    Listing Certified Through 2023-12-31

    Package

    NDC 63629-2680-03 (63629268003)

    NDC Package Code 63629-2680-3
    Billing NDC 63629268003
    Package 100 TABLET, FILM COATED in 1 BOTTLE (63629-2680-3)
    Marketing Start Date 2008-11-14
    NDC Exclude Flag N
    Pricing Information N/A