Package 62135-484-60
Brand: quinapril
Generic: quinaprilPackage Facts
Identity
Package NDC
62135-484-60
Digits Only
6213548460
Product NDC
62135-484
Description
60 TABLET, FILM COATED in 1 BOTTLE (62135-484-60)
Marketing
Marketing Status
Brand
quinapril
Generic
quinapril
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "09cd5cb9-4fdf-f133-e063-6294a90af691", "openfda": {"upc": ["0362135484606", "0362135487904", "0362135485900", "0362135486907"], "unii": ["33067B3N2M"], "rxcui": ["312748", "312749", "312750", "314203"], "spl_set_id": ["dbc43dbd-94aa-40e2-a9ea-766110cc8687"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (62135-484-60)", "package_ndc": "62135-484-60", "marketing_start_date": "20231106"}], "brand_name": "Quinapril", "product_id": "62135-484_09cd5cb9-4fdf-f133-e063-6294a90af691", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "62135-484", "generic_name": "Quinapril", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quinapril", "active_ingredients": [{"name": "QUINAPRIL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA076803", "marketing_category": "ANDA", "marketing_start_date": "20050302", "listing_expiration_date": "20261231"}