欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号PT/H/2610/001
药品名称Sunitinib Bluepharma
活性成分
    • SUNITINIB 12.5 mg
剂型Capsule, hard
上市许可持有人Bluepharma Genéricos - Comercio de Medicamentos, S.A
参考成员国 - 产品名称Portugal (PT)
互认成员国 - 产品名称
    • Poland (PL)
      Sunitinib Pharmascience
    • Hungary (HU)
      Sunitinib Pharmascience 12.5 mg kemény kapszula
    • Bulgaria (BG)
      Sunitinib Pharmascience
    • Cyprus (CY)
      Sunitinib Pharmascience 12.5mg hard capsules
    • Slovenia (SI)
    • Croatia (HR)
      Sunitinib Pharmascience 12,5 mg tvrde kapsule
许可日期2021/08/10
最近更新日期2024/06/28
药物ATC编码
    • L01XE04 sunitinib
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
附件文件下载
市场状态Positive
©2006-2024 Drugfuture->European Union HMA Authorisation of Medicines DataBase