quinapril

Generic: quinapril

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

Drug Facts

Product Profile

Brand Name quinapril
Generic Name quinapril
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

quinapril hydrochloride 10 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-635
Product ID 71205-635_91c30b32-c939-4f18-aa77-1f41d68a29e2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077690
Listing Expiration 2026-12-31
Marketing Start 2007-02-26

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 71205635
Hyphenated Format 71205-635

Supplemental Identifiers

RxCUI
312748
UPC
0371205635305
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 (source: ndc)
Application Number ANDA077690 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71205-635-30)
  • 60 TABLET in 1 BOTTLE (71205-635-60)
  • 90 TABLET in 1 BOTTLE (71205-635-90)
source: ndc

Packages (3)

71205-635-30 30 TABLET in 1 BOTTLE (71205-635-30) 71205-635-60 60 TABLET in 1 BOTTLE (71205-635-60) 71205-635-90 90 TABLET in 1 BOTTLE (71205-635-90)

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": "91c30b32-c939-4f18-aa77-1f41d68a29e2", "openfda": {"upc": ["0371205635305"], "unii": ["33067B3N2M"], "rxcui": ["312748"], "spl_set_id": ["2efb2ede-a49b-4e3e-9c93-4c202f67211f"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-635-30)", "package_ndc": "71205-635-30", "marketing_start_date": "20220131"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-635-60)", "package_ndc": "71205-635-60", "marketing_start_date": "20220131"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-635-90)", "package_ndc": "71205-635-90", "marketing_start_date": "20220131"}], "brand_name": "Quinapril", "product_id": "71205-635_91c30b32-c939-4f18-aa77-1f41d68a29e2", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "71205-635", "generic_name": "Quinapril", "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": "ANDA077690", "marketing_category": "ANDA", "marketing_start_date": "20070226", "listing_expiration_date": "20261231"}