欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号IE/H/1277/003
药品名称Cyclophosphamide 1 g Powder for solution for injection/infusion
活性成分
    • Cyclophosphamide 1.0 g
剂型Powder for solution for injection/infusion
上市许可持有人Seacross Pharma (Europe) Limited Pod 13, The Old Station House, 15a Main Street, Blackrock, Dublin, A94 T8P8, Ireland
参考成员国 - 产品名称Ireland (IE)
互认成员国 - 产品名称
    • Germany (DE)
      Cyclophosphamid Seacross 1g Pulver zur Herstellung einer Injektions-/Infusionslösung
    • Netherlands (NL)
      Cyclofosfamide Seacross 1000 mg poeder voor oplossing voor injectie/infusie
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
许可日期2024/10/23
最近更新日期2025/01/02
药物ATC编码
    • L01AA01 cyclophosphamide
申请类型
  • TypeLevel1：Known Active Substance
  • TypeLevel2：Initial Application
  • TypeLevel3：Generic
  • TypeLevel4：Chemical Substance
  • TypeLevel5：Prescription Only
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市场状态Positive
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