quinapril

Generic: quinapril hydrochloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name quinapril
Generic Name quinapril hydrochloride
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

quinapril hydrochloride 10 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-874
Product ID 63187-874_47f95e90-75fb-4294-b861-9a2349a48e91
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202725
Listing Expiration 2026-12-31
Marketing Start 2013-04-29

Pharmacologic Class

Classes
angiotensin converting enzyme inhibitor [epc] angiotensin-converting enzyme inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63187874
Hyphenated Format 63187-874

Supplemental Identifiers

RxCUI
312748
UNII
33067B3N2M

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name quinapril (source: ndc)
Generic Name quinapril hydrochloride (source: ndc)
Application Number ANDA202725 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (63187-874-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (63187-874-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (63187-874-90)
source: ndc

Packages (3)

63187-874-30 30 TABLET, FILM COATED in 1 BOTTLE (63187-874-30) 63187-874-60 60 TABLET, FILM COATED in 1 BOTTLE (63187-874-60) 63187-874-90 90 TABLET, FILM COATED in 1 BOTTLE (63187-874-90)

Ingredients (1)

quinapril hydrochloride (10 mg/1)

Linked Drug Pages (1)

Quinapril ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47f95e90-75fb-4294-b861-9a2349a48e91", "openfda": {"unii": ["33067B3N2M"], "rxcui": ["312748"], "spl_set_id": ["42e4f9dd-6032-4257-bd0f-8e9b71027f03"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63187-874-30)", "package_ndc": "63187-874-30", "marketing_start_date": "20170801"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (63187-874-60)", "package_ndc": "63187-874-60", "marketing_start_date": "20170801"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63187-874-90)", "package_ndc": "63187-874-90", "marketing_start_date": "20170801"}], "brand_name": "Quinapril", "product_id": "63187-874_47f95e90-75fb-4294-b861-9a2349a48e91", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "63187-874", "generic_name": "Quinapril Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quinapril", "active_ingredients": [{"name": "QUINAPRIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA202725", "marketing_category": "ANDA", "marketing_start_date": "20130429", "listing_expiration_date": "20261231"}