quinapril
Generic: quinapril hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
quinapril
Generic Name
quinapril hydrochloride
Labeler
bryant ranch prepack
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
quinapril hydrochloride 10 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
636297934
Hyphenated Format
63629-7934
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE (63629-7934-1)
Packages (1)
Ingredients (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"}