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    NDC 63187-0906-90 Benazepril Hydrochloride 40 mg/1 Details

    Benazepril Hydrochloride 40 mg/1

    Benazepril Hydrochloride is a ORAL TABLET, COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Proficient Rx LP. The primary component is BENAZEPRIL HYDROCHLORIDE.

    Product Information

    NDC 63187-0906
    Product ID 63187-906_9eeaae93-ac71-4721-98ad-8c7a9231f822
    Associated GPIs 36100005100340
    GCN Sequence Number 016042
    GCN Sequence Number Description benazepril HCl TABLET 40 MG ORAL
    HIC3 A4D
    HIC3 Description ANTIHYPERTENSIVES, ACE INHIBITORS
    GCN 48614
    HICL Sequence Number 006113
    HICL Sequence Number Description BENAZEPRIL HCL
    Brand/Generic Generic
    Proprietary Name Benazepril Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Benazepril Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, COATED
    Route ORAL
    Active Ingredient Strength 40
    Active Ingredient Units mg/1
    Substance Name BENAZEPRIL HYDROCHLORIDE
    Labeler Name Proficient Rx LP
    Pharmaceutical Class Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076118
    Listing Certified Through 2024-12-31

    Package

    NDC 63187-0906-90 (63187090690)

    NDC Package Code 63187-906-90
    Billing NDC 63187090690
    Package 90 TABLET, COATED in 1 BOTTLE (63187-906-90)
    Marketing Start Date 2017-09-01
    NDC Exclude Flag N
    Pricing Information N/A