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    NDC 68071-1026-06 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 NuCare Pharmaceuticals, Inc.. The primary component is BENAZEPRIL HYDROCHLORIDE.

    Product Information

    NDC 68071-1026
    Product ID 68071-1026_dcb81c38-2437-6c8e-e053-2995a90a85c7
    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 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 NuCare Pharmaceuticals, Inc.
    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 68071-1026-06 (68071102606)

    NDC Package Code 68071-1026-6
    Billing NDC 68071102606
    Package 60 TABLET, COATED in 1 BOTTLE (68071-1026-6)
    Marketing Start Date 2017-03-24
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 4b822870-e366-62d1-e054-00144ff88e88 Details

    Revised: 4/2022