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=BLA103948"
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
58468-0357-3 58468-0357 HUMAN PRESCRIPTION DRUG Campath ALEMTUZUMAB INJECTION INTRAVENOUS 20091130 N/A BLA BLA103948 Genzyme Corporation ALEMTUZUMAB 30 mg/mL 3 VIAL, SINGLE-USE in 1 CARTON (58468-0357-3) / 1 mL in 1 VIAL, SINGLE-USE
58468-0357-1 58468-0357 HUMAN PRESCRIPTION DRUG Campath ALEMTUZUMAB INJECTION INTRAVENOUS 20091130 N/A BLA BLA103948 Genzyme Corporation ALEMTUZUMAB 30 mg/mL 1 VIAL, SINGLE-USE in 1 CARTON (58468-0357-1) / 1 mL in 1 VIAL, SINGLE-USE
58468-0200-1 58468-0200 HUMAN PRESCRIPTION DRUG LEMTRADA ALEMTUZUMAB INJECTION, SOLUTION, CONCENTRATE INTRAVENOUS 20141118 N/A BLA BLA103948 Genzyme Corporation ALEMTUZUMAB 12 mg/1.2mL 1 VIAL, SINGLE-USE in 1 CARTON (58468-0200-1) / 1.2 mL in 1 VIAL, SINGLE-USE
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase