Package 80005-129-08
Brand: aminocaproic acid
Generic: aminocaproic acidPackage Facts
Identity
Package NDC
80005-129-08
Digits Only
8000512908
Product NDC
80005-129
Description
30 TABLET in 1 BOTTLE (80005-129-08)
Marketing
Marketing Status
Brand
aminocaproic acid
Generic
aminocaproic acid
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "98b3715d-7fcf-4802-8b34-c1296b03b5fb", "openfda": {"nui": ["N0000175634", "N0000175632"], "upc": ["0380005128085"], "unii": ["U6F3787206"], "rxcui": ["197351", "476271"], "spl_set_id": ["871ec401-30f8-4154-a16e-b82dc1e04b49"], "pharm_class_pe": ["Decreased Fibrinolysis [PE]"], "pharm_class_epc": ["Antifibrinolytic Agent [EPC]"], "manufacturer_name": ["Carnegie Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (80005-129-08)", "package_ndc": "80005-129-08", "marketing_start_date": "20210315"}], "brand_name": "AMINOCAPROIC ACID", "product_id": "80005-129_98b3715d-7fcf-4802-8b34-c1296b03b5fb", "dosage_form": "TABLET", "pharm_class": ["Antifibrinolytic Agent [EPC]", "Decreased Fibrinolysis [PE]"], "product_ndc": "80005-129", "generic_name": "AMINOCAPROIC ACID", "labeler_name": "Carnegie Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMINOCAPROIC ACID", "active_ingredients": [{"name": "AMINOCAPROIC ACID", "strength": "1000 mg/1"}], "application_number": "ANDA213928", "marketing_category": "ANDA", "marketing_start_date": "20210315", "listing_expiration_date": "20261231"}