Package 71335-1134-1

Brand: quinapril

Generic: quinapril
NDC Package

Package Facts

Identity

Package NDC 71335-1134-1
Digits Only 7133511341
Product NDC 71335-1134
Product ID 71335-1134_fda04907-70de-68d6-e053-6394a90a00d6
Description

30 TABLET in 1 BOTTLE (71335-1134-1)

Marketing

Marketing Status
Marketed Since 2019-11-08
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": "fda04907-70de-68d6-e053-6394a90a00d6", "openfda": {"unii": ["33067B3N2M"], "rxcui": ["312748"], "spl_set_id": ["fb069caa-14d0-4f76-b662-6145fb4cc276"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1134-1)", "package_ndc": "71335-1134-1", "marketing_start_date": "20191108"}], "brand_name": "QUINAPRIL", "product_id": "71335-1134_fda04907-70de-68d6-e053-6394a90a00d6", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "71335-1134", "generic_name": "quinapril", "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": "ANDA205823", "marketing_category": "ANDA", "marketing_start_date": "20171110", "listing_expiration_date": "20261231"}