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
60760-604-90	60760-604	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191016	N/A	ANDA	ANDA090796	St. Mary's Medical Park Pharmacy	IBUPROFEN	800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-604-90)
51655-474-25	51655-474	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20201113	N/A	ANDA	ANDA090796	Northwind Health Company, LLC	IBUPROFEN	600 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-474-25)
51655-474-26	51655-474	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20220621	N/A	ANDA	ANDA090796	Northwind Health Company, LLC	IBUPROFEN	600 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-474-26)
51655-474-51	51655-474	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20210208	N/A	ANDA	ANDA090796	Northwind Health Company, LLC	IBUPROFEN	600 mg/1	40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-474-51)
73086-211-01	73086-211	HUMAN PRESCRIPTION DRUG	ibuprofen	ibuprofen	TABLET	ORAL	20240320	N/A	ANDA	ANDA090796	SKYA HEALTH, LLC	IBUPROFEN	600 mg/1	100 TABLET in 1 BOTTLE (73086-211-01)
73086-212-01	73086-212	HUMAN PRESCRIPTION DRUG	ibuprofen	ibuprofen	TABLET	ORAL	20240320	N/A	ANDA	ANDA090796	SKYA HEALTH, LLC	IBUPROFEN	800 mg/1	100 TABLET in 1 BOTTLE (73086-212-01)
73086-210-01	73086-210	HUMAN PRESCRIPTION DRUG	ibuprofen	ibuprofen	TABLET	ORAL	20240320	N/A	ANDA	ANDA090796	SKYA HEALTH, LLC	IBUPROFEN	400 mg/1	100 TABLET in 1 BOTTLE (73086-210-01)