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
68071-5140-6	68071-5140	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200106	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	800 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (68071-5140-6)
25000-121-03	25000-121	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20110228	N/A	ANDA	ANDA090796	MARKSANS PHARMA LIMITED	IBUPROFEN	400 mg/1	30 TABLET in 1 BOTTLE (25000-121-03)
25000-121-12	25000-121	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20110228	N/A	ANDA	ANDA090796	MARKSANS PHARMA LIMITED	IBUPROFEN	400 mg/1	500 TABLET in 1 BOTTLE (25000-121-12)
25000-122-03	25000-122	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20110228	N/A	ANDA	ANDA090796	MARKSANS PHARMA LIMITED	IBUPROFEN	600 mg/1	30 TABLET in 1 BOTTLE (25000-122-03)
25000-122-12	25000-122	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20110228	N/A	ANDA	ANDA090796	MARKSANS PHARMA LIMITED	IBUPROFEN	600 mg/1	500 TABLET in 1 BOTTLE (25000-122-12)
25000-123-03	25000-123	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20110228	N/A	ANDA	ANDA090796	MARKSANS PHARMA LIMITED	IBUPROFEN	800 mg/1	30 TABLET in 1 BOTTLE (25000-123-03)
25000-123-12	25000-123	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20110228	N/A	ANDA	ANDA090796	MARKSANS PHARMA LIMITED	IBUPROFEN	800 mg/1	500 TABLET in 1 BOTTLE (25000-123-12)