欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/5167/001
药品名称Sorafenib Sandoz 400 mg film-coated tablet
活性成分
    • SORAFENIB TOSILATE 400.0 mg
剂型Film-coated tablet
上市许可持有人Sandoz B.V. Veluwezoom 22, 1327 AH Almere, The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Sorafenib Sandoz 400 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Estonia (EE)
    • Hungary (HU)
      Sorafenib Sandoz 400 mg filmtabletta
    • Germany (DE)
      Sorafenib HEXAL 400 mg Filmtabletten
    • Czechia (CZ)
      Sorafenib Sandoz
    • Denmark (DK)
    • Romania (RO)
    • Belgium (BE)
      Sorafenib Sandoz 400 mg filmomhulde tabletten
    • Slovakia (SK)
    • Austria (AT)
      Sorafenib Sandoz 400 mg - Filmtabletten
    • Croatia (HR)
    • Spain (ES)
    • Portugal (PT)
    • Greece (GR)
    • Poland (PL)
      Sorafenib Sandoz
    • Latvia (LV)
      Sorafenib Sandoz 400 mg apvalkotās tabletes
    • Lithuania (LT)
      Sorafenib Ebewe 400 mg plėvele dengtos tabletės
许可日期2021/04/29
最近更新日期2023/12/15
药物ATC编码
    • L01EX02 sorafenib
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Initial Application
  • TypeLevel3:Other Generic application Art 10.3 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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