欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DK/H/3068/001
药品名称Sunitinib Sigillata
活性成分
    • SUNITINIB 12.5 mg
剂型Capsule, hard
上市许可持有人Sigillata Ltd. Block A 15 Castleforbes Square Sheriff Street Dublin 1 Ireland
参考成员国 - 产品名称Denmark (DK)
互认成员国 - 产品名称
    • Germany (DE)
      Sunitinib Sigillata 12,5 mg Hartkapseln
许可日期2021/04/12
最近更新日期2021/04/13
药物ATC编码
    • L01XE04 sunitinib
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Withdrawn(注:已撤市)
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