欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号IE/H/0742/001
药品名称lrinotecan 20 mg/ml Solutionfor Infusion 40 mg/2 ml and 100 mg/S ml Vials
活性成分
    • irinotecan hydrochloride 20.0 mg/ml
剂型Solution for infusion
上市许可持有人Fresenius Kabi Oncology Plc Lion Court Farnham Road Bordon Hampshire GU35 ONF United Kingdom
参考成员国 - 产品名称Ireland (IE)
互认成员国 - 产品名称
    • United Kingdom (Northern Ireland) (XI)
    • Denmark (DK)
    • Spain (ES)
    • Italy (IT)
    • Finland (FI)
    • Latvia (LV)
    • Lithuania (LT)
      Irinotecan Dabur 20 mg/ml infuzinis tirpalas
    • Estonia (EE)
    • Hungary (HU)
      Irinotecan-Dabur old. inf. 20mg/ml
    • Czechia (CZ)
    • Slovakia (SK)
      Irinotecan 20mg/ml infúzny intravenózmy roztok
    • Poland (PL)
许可日期2008/04/05
最近更新日期2024/04/11
药物ATC编码
    • L01XX19 irinotecan
申请类型
  • TypeLevel1:[not specified]
  • TypeLevel2:[not specified]
  • TypeLevel3:[not specified]
  • TypeLevel4:[not specified]
  • TypeLevel5:[not specified]
附件文件下载
    市场状态Positive
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