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    NDC 61919-0970-30 LISINOPRIL AND HYDROCHLOROTHIAZIDE 12.5; 10 mg/1; mg/1 Details

    LISINOPRIL AND HYDROCHLOROTHIAZIDE 12.5; 10 mg/1; mg/1

    LISINOPRIL AND HYDROCHLOROTHIAZIDE is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by DirectRx. The primary component is HYDROCHLOROTHIAZIDE; LISINOPRIL.

    Product Information

    NDC 61919-0970
    Product ID 61919-970_f2162166-3d61-392f-e053-2a95a90a8fc1
    Associated GPIs 36991802550305
    GCN Sequence Number 021277
    GCN Sequence Number Description lisinopril/hydrochlorothiazide TABLET 10-12.5 MG ORAL
    HIC3 A4J
    HIC3 Description ACE INHIBITOR-THIAZIDE OR THIAZIDE-LIKE DIURETIC
    GCN 88002
    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 12.5; 10
    Active Ingredient Units mg/1; mg/1
    Substance Name HYDROCHLOROTHIAZIDE; LISINOPRIL
    Labeler Name DirectRx
    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 61919-0970-30 (61919097030)

    NDC Package Code 61919-970-30
    Billing NDC 61919097030
    Package 30 TABLET in 1 BOTTLE (61919-970-30)
    Marketing Start Date 2021-09-02
    NDC Exclude Flag N
    Pricing Information N/A