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
68788-9112-7	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)
68788-9110-5	68788-9110	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20081120	N/A	ANDA	ANDA075682	Preferred Pharmaceuticals, Inc.	IBUPROFEN	400 mg/1	50 TABLET in 1 BOTTLE (68788-9110-5)
68788-9110-1	68788-9110	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20081120	N/A	ANDA	ANDA075682	Preferred Pharmaceuticals, Inc.	IBUPROFEN	400 mg/1	100 TABLET in 1 BOTTLE (68788-9110-1)
68788-9110-2	68788-9110	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20081120	N/A	ANDA	ANDA075682	Preferred Pharmaceuticals, Inc.	IBUPROFEN	400 mg/1	20 TABLET in 1 BOTTLE (68788-9110-2)