Package 63629-7934-1

Brand: quinapril

Generic: quinapril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-7934-1
Digits Only 6362979341
Product NDC 63629-7934
Product ID 63629-7934_03c7c1b9-9bf2-432b-8ed4-31df80eb340e
Description

30 TABLET, FILM COATED in 1 BOTTLE (63629-7934-1)

Marketing

Marketing Status
Marketed Since 2019-03-01
Brand quinapril
Generic quinapril hydrochloride
Sample Package No

Linked Drug Pages (1)

Quinapril ndc-match (0.95)

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"}