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)
检索条件:" 注册申请号=NDA203341"
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
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)
63539-117-01 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)
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)
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