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
63539-117-01	63539-117	HUMAN PRESCRIPTION DRUG	BOSULIF	Bosutinib	TABLET, FILM COATED	ORAL	20120904	N/A	NDA	NDA203341	U.S. Pharmaceuticals	BOSUTINIB MONOHYDRATE	100 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (63539-117-01)
0069-0136-01	0069-0136	HUMAN PRESCRIPTION DRUG	BOSULIF	Bosutinib	TABLET, FILM COATED	ORAL	20120904	N/A	NDA	NDA203341	Pfizer Laboratories Div Pfizer Inc	BOSUTINIB MONOHYDRATE	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0069-0136-01)
0069-0135-01	0069-0135	HUMAN PRESCRIPTION DRUG	BOSULIF	Bosutinib	TABLET, FILM COATED	ORAL	20120904	N/A	NDA	NDA203341	Pfizer Laboratories Div Pfizer Inc	BOSUTINIB MONOHYDRATE	100 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (0069-0135-01)
0069-0193-01	0069-0193	HUMAN PRESCRIPTION DRUG	BOSULIF	Bosutinib	TABLET, FILM COATED	ORAL	20171218	N/A	NDA	NDA203341	Pfizer Laboratories Div Pfizer Inc	BOSUTINIB MONOHYDRATE	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0069-0193-01)
63539-193-30	63539-193	HUMAN PRESCRIPTION DRUG	BOSULIF	Bosutinib	TABLET, FILM COATED	ORAL	20180221	N/A	NDA	NDA203341	U.S. Pharmaceuticals	BOSUTINIB MONOHYDRATE	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63539-193-30)