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    NDC 63187-0257-30 Lisinopril 20 mg/1 Details

    Lisinopril 20 mg/1

    Lisinopril is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Proficient Rx LP. The primary component is LISINOPRIL.

    Product Information

    NDC 63187-0257
    Product ID 63187-257_f0c279c5-1f67-4d03-ba2d-6202d619299c
    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 Lisinopril
    Proprietary Name Suffix n/a
    Non-Proprietary Name Lisinopril
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name LISINOPRIL
    Labeler Name Proficient Rx LP
    Pharmaceutical Class Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077321
    Listing Certified Through 2024-12-31

    Package

    NDC 63187-0257-30 (63187025730)

    NDC Package Code 63187-257-30
    Billing NDC 63187025730
    Package 30 TABLET in 1 BOTTLE (63187-257-30)
    Marketing Start Date 2016-08-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL d87620e1-1a43-43a2-ab37-b9111ea5c17e Details

    Revised: 11/2019