欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号SE/H/2271/001
药品名称Sorafenib Mylan
活性成分
    • SORAFENIB TOSILATE 200.0 mg
剂型Film-coated tablet
上市许可持有人Mylan AB Sweden
参考成员国 - 产品名称Sweden (SE)
互认成员国 - 产品名称
    • Norway (NO)
    • Germany (DE)
      Sorel 200 mg Filmtabletten
    • Denmark (DK)
    • Iceland (IS)
      Sorafenib Mylan 200 mg Filmuhúðuð tafla
    • United Kingdom (Northern Ireland) (XI)
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Finland (FI)
    • Poland (PL)
      Sorafenib Mylan
    • Bulgaria (BG)
      Sorel
    • Czechia (CZ)
      Sorel
    • Romania (RO)
      Sorel 200 mg comprimate filmate
    • Croatia (HR)
      Sorafenib Mylan 200 mg filmom obložene tablete
许可日期2020/06/05
最近更新日期2023/12/20
药物ATC编码
    • L01XE05 sorafenib
申请类型
  • TypeLevel1:[not specified]
  • TypeLevel2:[not specified]
  • TypeLevel3:[not specified]
  • TypeLevel4:[not specified]
  • TypeLevel5:[not specified]
附件文件下载
市场状态Positive
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