欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号FI/H/0238/001
药品名称Irinotecan Mayne 20 mg/ml
活性成分
    • irinotecan hydrochloride 20.0 mg/ml
剂型Concentrate for solution for infusion
上市许可持有人Mayne Pharma Plc
参考成员国 - 产品名称Finland (FI)
互认成员国 - 产品名称
    • Denmark (DK)
      Irinotecan "Mayne"
    • Iceland (IS)
    • Ireland (IE)
    • Spain (ES)
      Irinotecan Rovi 20 mg/ml concentrado para solución para perfusió
    • Portugal (PT)
    • Greece (GR)
    • Norway (NO)
    • Austria (AT)
      Irinotecan Mayne 20 mg/ml - Konzentrat zur Herstellung einer Infusionslösung
    • Poland (PL)
    • Latvia (LV)
      Irinotecan Mayne 20 mg/ml
    • Hungary (HU)
      Irinotecan Mayne
    • Cyprus (CY)
      Irinotecan Hydrochloride 20 mg/ml concentrate for solution for infusion
    • Czechia (CZ)
      Canri
    • Slovakia (SK)
      IRINOTECAN MAYNE 20mg/ml infúzny koncentrát
    • Italy (IT)
许可日期2003/12/18
最近更新日期2019/01/30
药物ATC编码
    • L ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
    • L01 ANTINEOPLASTIC AGENTS
    • L01X OTHER ANTINEOPLASTIC AGENTS
    • L01XX Other antineoplastic agents
    • L01XX19 irinotecan
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Initial Application
  • TypeLevel3:Generic Article 4.8(a)(iii), first paragraph
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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    市场状态Positive
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