欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/2814/001
药品名称Cyclofosfamide Cadiasun 500 mg
活性成分
    • cyclophosphamide 500.0 mg
剂型Powder for solution for injection
上市许可持有人Cadiasun Pharma GmbH Lendersweg 27, 47877 Willich Germany
参考成员国 - 产品名称Netherlands (NL)
Cyclofosfamide Cadiasun 500 mg, poeder voor oplossing voor injectie
互认成员国 - 产品名称
    许可日期2014/05/28
    最近更新日期2022/01/22
    药物ATC编码
      • L01AA01 cyclophosphamide
    申请类型
    • TypeLevel1:Known Active Substance
    • TypeLevel2:Initial Application
    • TypeLevel3:Generic Art 10.1 and 10.2 Dir 2001/83/EC
    • TypeLevel4:Chemical Substance
    • TypeLevel5:Prescription Only
    附件文件下载
    市场状态Withdrawn(注:已撤市)
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