欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DK/H/3198/001
药品名称Icatibant Glenmark
活性成分
    • icatibant acetate 10.0 mg/ml
剂型Solution for injection in pre-filled syringe
上市许可持有人Glenmark Arzneimittel GmbH, Industriestraße 31, Gröbenzell, Bayern, 82194 Germany
参考成员国 - 产品名称Denmark (DK)
Icatibant Glenmark
互认成员国 - 产品名称
    • Germany (DE)
      Icatibant Glenmark 30 mg/3 ml Injektionslösung in einer Fertigspritze
    • Netherlands (NL)
      Icatibant Glenmark 30 mg oplossing voor injectie in een voorgevulde spuit
    • Spain (ES)
    • Sweden (SE)
    • Norway (NO)
      Icatibant Glenmark
    • Finland (FI)
    • Czechia (CZ)
      Icatibant Glenmark
    • Slovakia (SK)
      Icatibant Glenmark 30 mginjekčný roztok v naplnenej injekčnej striekačke
许可日期2021/09/08
最近更新日期2024/04/18
药物ATC编码
    • B06AC02 icatibant
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Multiple (Copy) 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Positive
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