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=NDA022291"
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
0078-0684-15 0078-0684 HUMAN PRESCRIPTION DRUG PROMACTA eltrombopag olamine TABLET, FILM COATED ORAL 20160822 N/A NDA NDA022291 Novartis Pharmaceuticals Corporation ELTROMBOPAG OLAMINE 12.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0078-0684-15)
0078-0685-15 0078-0685 HUMAN PRESCRIPTION DRUG PROMACTA eltrombopag olamine TABLET, FILM COATED ORAL 20160524 N/A NDA NDA022291 Novartis Pharmaceuticals Corporation ELTROMBOPAG OLAMINE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0078-0685-15)
0078-0686-15 0078-0686 HUMAN PRESCRIPTION DRUG PROMACTA eltrombopag olamine TABLET, FILM COATED ORAL 20160407 N/A NDA NDA022291 Novartis Pharmaceuticals Corporation ELTROMBOPAG OLAMINE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0078-0686-15)
0078-0686-55 0078-0686 HUMAN PRESCRIPTION DRUG PROMACTA eltrombopag olamine TABLET, FILM COATED ORAL 20200121 N/A NDA NDA022291 Novartis Pharmaceuticals Corporation ELTROMBOPAG OLAMINE 50 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (0078-0686-55)
0078-0687-15 0078-0687 HUMAN PRESCRIPTION DRUG PROMACTA eltrombopag olamine TABLET, FILM COATED ORAL 20160401 N/A NDA NDA022291 Novartis Pharmaceuticals Corporation ELTROMBOPAG OLAMINE 75 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0078-0687-15)
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