Package 63629-8710-1

Brand: quinapril

Generic: quinapril
NDC Package

Package Facts

Identity

Package NDC 63629-8710-1
Digits Only 6362987101
Product NDC 63629-8710
Product ID 63629-8710_78872c13-1caa-4a0f-9f5e-995fcfb35e73
Description

30 TABLET in 1 BOTTLE (63629-8710-1)

Marketing

Marketing Status
Marketed Since 2021-08-02
Brand quinapril
Generic quinapril
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": "78872c13-1caa-4a0f-9f5e-995fcfb35e73", "openfda": {"unii": ["33067B3N2M"], "rxcui": ["312749"], "spl_set_id": ["da84cb14-a9dd-4df0-a7e5-d5fbd84ac6da"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-8710-1)", "package_ndc": "63629-8710-1", "marketing_start_date": "20210802"}], "brand_name": "QUINAPRIL", "product_id": "63629-8710_78872c13-1caa-4a0f-9f5e-995fcfb35e73", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "63629-8710", "generic_name": "quinapril", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "QUINAPRIL", "active_ingredients": [{"name": "QUINAPRIL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA205823", "marketing_category": "ANDA", "marketing_start_date": "20171110", "listing_expiration_date": "20261231"}