Search by Drug Name or NDC

    NDC 71205-0635-30 Quinapril 10 mg/1 Details

    Quinapril 10 mg/1

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

    Product Information

    NDC 71205-0635
    Product ID 71205-635_91c30b32-c939-4f18-aa77-1f41d68a29e2
    Associated GPIs 36100040100310
    GCN Sequence Number 018772
    GCN Sequence Number Description quinapril HCl TABLET 10 MG ORAL
    HIC3 A4D
    HIC3 Description ANTIHYPERTENSIVES, ACE INHIBITORS
    GCN 27570
    HICL Sequence Number 007631
    HICL Sequence Number Description QUINAPRIL HCL
    Brand/Generic Generic
    Proprietary Name Quinapril
    Proprietary Name Suffix n/a
    Non-Proprietary Name Quinapril
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 10
    Active Ingredient Units mg/1
    Substance Name QUINAPRIL HYDROCHLORIDE
    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 ANDA077690
    Listing Certified Through 2024-12-31

    Package

    NDC 71205-0635-30 (71205063530)

    NDC Package Code 71205-635-30
    Billing NDC 71205063530
    Package 30 TABLET in 1 BOTTLE (71205-635-30)
    Marketing Start Date 2022-01-31
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 2efb2ede-a49b-4e3e-9c93-4c202f67211f Details

    Revised: 5/2022