Package 69097-842-15

Brand: quinapril

Generic: quinapril
NDC Package

Package Facts

Identity

Package NDC 69097-842-15
Digits Only 6909784215
Product NDC 69097-842
Product ID 69097-842_56ce107f-65d9-4ec8-8859-6a256b27dc57
Description

1000 TABLET in 1 BOTTLE (69097-842-15)

Marketing

Marketing Status
Marketed Since 2016-07-22
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": "56ce107f-65d9-4ec8-8859-6a256b27dc57", "openfda": {"upc": ["0369097841058", "0369097839055", "0369097842055", "0369097843052"], "unii": ["33067B3N2M"], "rxcui": ["312748", "312749", "312750", "314203"], "spl_set_id": ["e6d36e1e-8e35-4d06-83dc-45e0456365fd"], "manufacturer_name": ["Cipla USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (69097-842-05)", "package_ndc": "69097-842-05", "marketing_start_date": "20160722"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (69097-842-15)", "package_ndc": "69097-842-15", "marketing_start_date": "20160722"}], "brand_name": "Quinapril", "product_id": "69097-842_56ce107f-65d9-4ec8-8859-6a256b27dc57", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "69097-842", "generic_name": "Quinapril", "labeler_name": "Cipla USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quinapril", "active_ingredients": [{"name": "QUINAPRIL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA078457", "marketing_category": "ANDA", "marketing_start_date": "20160722", "listing_expiration_date": "20261231"}