欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号AT/H/1093/001
药品名称Levosimendan Amdipharm 2,5 mg/ml Konzentrat zur Herstellung einer Infusionslösung
活性成分
    • levosimendan 2.5 mg/ml
剂型Concentrate for solution for infusion
上市许可持有人Amdipharm Limited Burleigh Mews, 3 Burlington Road, Ballsbridge Dublin, Ireland
参考成员国 - 产品名称Austria (AT)
互认成员国 - 产品名称
    • Denmark (DK)
      Levosimendan ”Amdipharm”
    • Sweden (SE)
    • Norway (NO)
      Levosimendan Amdipharm
    • Finland (FI)
许可日期2021/12/13
最近更新日期2024/06/06
药物ATC编码
    • C01CX08 levosimendan
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Initial Application
  • TypeLevel3:Generic Art 10.1 and 10.2 Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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