美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
0143-9432-27	0143-9432	HUMAN PRESCRIPTION DRUG	Combogesic	ACETAMINOPHEN and IBUPROFEN	TABLET, FILM COATED	ORAL	20250106	N/A	NDA	NDA209471	Hikma Pharmaceuticals USA Inc	ACETAMINOPHEN; IBUPROFEN	325 mg/1; 97.5 mg/1	250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0143-9432-27)
72260-129-01	72260-129	HUMAN PRESCRIPTION DRUG	Combogesic	ACETAMINOPHEN and IBUPROFEN	TABLET, FILM COATED	ORAL	20250106	N/A	NDA	NDA209471	AFT Pharmaceuticals US, Inc.	ACETAMINOPHEN; IBUPROFEN	325 mg/1; 97.5 mg/1	250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72260-129-01)
68788-4009-1	68788-4009	HUMAN PRESCRIPTION DRUG	Combogesic	ACETAMINOPHEN and IBUPROFEN	TABLET, FILM COATED	ORAL	20250904	N/A	NDA	NDA209471	Preferred Pharmaceuticals Inc.	ACETAMINOPHEN; IBUPROFEN	325 mg/1; 97.5 mg/1	120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4009-1)