Package 0904-7485-03

Brand: febuxostat

Generic: febuxostat
NDC Package

Package Facts

Identity

Package NDC 0904-7485-03
Digits Only 0904748503
Product NDC 0904-7485
Description

30 TABLET, FILM COATED in 1 BOTTLE (0904-7485-03)

Marketing

Marketing Status
Discontinued 2026-08-31
Brand febuxostat
Generic febuxostat
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2bc97ac5-e672-4bb9-b0c4-596bbe935292", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["101V0R1N2E"], "rxcui": ["834235", "834241"], "spl_set_id": ["164feabd-f722-445b-b81a-d975b3db5f53"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0904-7485-03)", "package_ndc": "0904-7485-03", "marketing_end_date": "20260831", "marketing_start_date": "20240522"}], "brand_name": "Febuxostat", "product_id": "0904-7485_2bc97ac5-e672-4bb9-b0c4-596bbe935292", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "0904-7485", "generic_name": "Febuxostat", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Febuxostat", "active_ingredients": [{"name": "FEBUXOSTAT", "strength": "80 mg/1"}], "application_number": "ANDA210461", "marketing_category": "ANDA", "marketing_end_date": "20260831", "marketing_start_date": "20240522"}