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    NDC 63629-3739-02 Lisinopril and Hydrochlorothiazide 25; 20 mg/1; mg/1 Details

    Lisinopril and Hydrochlorothiazide 25; 20 mg/1; mg/1

    Lisinopril and Hydrochlorothiazide is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is HYDROCHLOROTHIAZIDE; LISINOPRIL.

    Product Information

    NDC 63629-3739
    Product ID 63629-3739_1009900e-6a3d-4e8d-a533-334e0bfca2c2
    Associated GPIs 36991802550320
    GCN Sequence Number 000389
    GCN Sequence Number Description lisinopril/hydrochlorothiazide TABLET 20 MG-25MG ORAL
    HIC3 A4J
    HIC3 Description ACE INHIBITOR-THIAZIDE OR THIAZIDE-LIKE DIURETIC
    GCN 88001
    HICL Sequence Number 000131
    HICL Sequence Number Description LISINOPRIL/HYDROCHLOROTHIAZIDE
    Brand/Generic Generic
    Proprietary Name Lisinopril and Hydrochlorothiazide
    Proprietary Name Suffix n/a
    Non-Proprietary Name Lisinopril and Hydrochlorothiazide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 25; 20
    Active Ingredient Units mg/1; mg/1
    Substance Name HYDROCHLOROTHIAZIDE; LISINOPRIL
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077912
    Listing Certified Through 2024-12-31

    Package

    NDC 63629-3739-02 (63629373902)

    NDC Package Code 63629-3739-2
    Billing NDC 63629373902
    Package 60 TABLET in 1 BOTTLE (63629-3739-2)
    Marketing Start Date 2011-10-06
    NDC Exclude Flag N
    Pricing Information N/A