欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DK/H/3228/001
药品名称Icatibant GP Pharm
活性成分
    • icatibant acetate 30.0 mg/ml
剂型Solution for injection in pre-filled syringe
上市许可持有人GP-Pharm S.A., Plaça Europa 9-11, Planta 13, L'hospitalet De Llobregat, 08908 Barcelona Spain
参考成员国 - 产品名称Denmark (DK)
Icatibant GP Pharm
互认成员国 - 产品名称
    • Italy (IT)
    • Germany (DE)
      Icatibant GP Pharm 30 mg Injektionslösung in einer Fertigspritze
    • France (FR)
    • Spain (ES)
许可日期2022/01/13
最近更新日期2022/04/21
药物ATC编码
    • B06AC02 icatibant
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial 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
©2006-2024 Drugfuture->European Union HMA Authorisation of Medicines DataBase