quinapril

Generic: quinapril hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name quinapril
Generic Name quinapril hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

quinapril hydrochloride 10 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 63629-7934
Product ID 63629-7934_03c7c1b9-9bf2-432b-8ed4-31df80eb340e
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 636297934
Hyphenated Format 63629-7934

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 (63629-7934-1)
source: ndc

Packages (1)

Ingredients (1)

quinapril hydrochloride (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "03c7c1b9-9bf2-432b-8ed4-31df80eb340e", "openfda": {"unii": ["33067B3N2M"], "rxcui": ["312748"], "spl_set_id": ["a62d0ed3-8fcc-45fb-9246-b57b08a11f60"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63629-7934-1)", "package_ndc": "63629-7934-1", "marketing_start_date": "20190301"}], "brand_name": "Quinapril", "product_id": "63629-7934_03c7c1b9-9bf2-432b-8ed4-31df80eb340e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "63629-7934", "generic_name": "Quinapril Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "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"}