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    NDC 43063-0482-30 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 PD-Rx Pharmaceuticals, Inc.. The primary component is HYDROCHLOROTHIAZIDE; LISINOPRIL.

    Product Information

    NDC 43063-0482
    Product ID 43063-482_fb5bdef3-130a-9a52-e053-6294a90a1054
    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 PD-Rx Pharmaceuticals, Inc.
    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 43063-0482-30 (43063048230)

    NDC Package Code 43063-482-30
    Billing NDC 43063048230
    Package 30 TABLET in 1 BOTTLE, PLASTIC (43063-482-30)
    Marketing Start Date 2013-07-02
    NDC Exclude Flag N
    Pricing Information N/A