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    NDC 42708-0032-30 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 QPharma Inc. The primary component is LISINOPRIL.

    Product Information

    NDC 42708-0032
    Product ID 42708-032_f27a52d9-7058-ac2b-e053-2a95a90a32ac
    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 QPharma Inc
    Pharmaceutical Class Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076059
    Listing Certified Through 2024-12-31

    Package

    NDC 42708-0032-30 (42708003230)

    NDC Package Code 42708-032-30
    Billing NDC 42708003230
    Package 30 TABLET in 1 BOTTLE, PLASTIC (42708-032-30)
    Marketing Start Date 2018-03-14
    NDC Exclude Flag N
    Pricing Information N/A