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
68788-9112-6	68788-9112	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20081120	N/A	ANDA	ANDA075682	Preferred Pharmaceuticals, Inc.	IBUPROFEN	800 mg/1	60 TABLET in 1 BOTTLE (68788-9112-6)
68788-9112-7	68788-9112	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20081120	N/A	ANDA	ANDA075682	Preferred Pharmaceuticals, Inc.	IBUPROFEN	800 mg/1	21 TABLET in 1 BOTTLE (68788-9112-7)
68788-9112-8	68788-9112	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20081120	N/A	ANDA	ANDA075682	Preferred Pharmaceuticals, Inc.	IBUPROFEN	800 mg/1	120 TABLET in 1 BOTTLE (68788-9112-8)
68788-9112-9	68788-9112	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20081120	N/A	ANDA	ANDA075682	Preferred Pharmaceuticals, Inc.	IBUPROFEN	800 mg/1	90 TABLET in 1 BOTTLE (68788-9112-9)
66267-963-00	66267-963	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20170915	N/A	ANDA	ANDA075682	NuCare Pharmaceuticals,Inc.	IBUPROFEN	800 mg/1	100 TABLET in 1 BOTTLE (66267-963-00)
66267-964-00	66267-964	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20170822	N/A	ANDA	ANDA075682	NuCare Pharmaceuticals Inc.	IBUPROFEN	600 mg/1	100 TABLET in 1 BOTTLE (66267-964-00)