欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/4973/001
药品名称Sunitinib Zentiva 12,5, harde capsules.
活性成分
    • SUNITINIB 12.5 mg
剂型Capsule, hard
上市许可持有人Zentiva k.s. U kabelovny 130, Dolní Měcholupy Prague 10, 102 37 Czech Republic
参考成员国 - 产品名称Netherlands (NL)
Sunitinib Zentiva 12,5 mg, harde capsules
互认成员国 - 产品名称
    • Germany (DE)
    • Denmark (DK)
    • United Kingdom (Northern Ireland) (XI)
    • France (FR)
    • Italy (IT)
    • Sweden (SE)
    • Poland (PL)
    • Latvia (LV)
      Sunitinib Zentiva 12,5 mg cietās kapsulas
    • Lithuania (LT)
      Sunitinib Zentiva 12,5 mg kietosios kapsulės
    • Estonia (EE)
      SUNITINIB ZENTIVA
    • Bulgaria (BG)
      Sunitinib Zentiva
    • Czechia (CZ)
      Sunitinib Zentiva
    • Romania (RO)
      Sunitinib Zentiva 12,5 mg capsule
    • Slovakia (SK)
许可日期2020/10/29
最近更新日期2024/08/14
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
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