Package 43547-412-09

Brand: quinapril

Generic: quinapril
NDC Package

Package Facts

Identity

Package NDC 43547-412-09
Digits Only 4354741209
Product NDC 43547-412
Product ID 43547-412_b8f1731a-cbac-4f64-a8d4-320b80b335e1
Description

90 TABLET in 1 BOTTLE (43547-412-09)

Marketing

Marketing Status
Marketed Since 2017-11-10
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": "b8f1731a-cbac-4f64-a8d4-320b80b335e1", "openfda": {"unii": ["33067B3N2M"], "rxcui": ["312748", "312749", "312750", "314203"], "spl_set_id": ["cd46691d-5593-4a9f-a937-999c6803e312"], "manufacturer_name": ["Solco Healthcare US, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (43547-412-09)", "package_ndc": "43547-412-09", "marketing_start_date": "20171110"}], "brand_name": "QUINAPRIL", "product_id": "43547-412_b8f1731a-cbac-4f64-a8d4-320b80b335e1", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "43547-412", "generic_name": "quinapril", "labeler_name": "Solco Healthcare US, LLC", "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"}