欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/5984/003
药品名称Xintev 15 mg, film-coated tablets
活性成分
    • Vortioxetin hydrobromide 15.0 mg
剂型Film-coated tablet
上市许可持有人Viatris Limited Damastown Industrial Park 15 Dublin Ireland
参考成员国 - 产品名称Netherlands (NL)
Xintev 15 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Portugal (PT)
    • Greece (GR)
    • Poland (PL)
      Vortioxetine Viatris Pharma
    • Hungary (HU)
      Xintev 15 mg filmtabletta
    • Croatia (HR)
许可日期2025/03/14
最近更新日期2025/03/18
药物ATC编码
    • N06AX26 vortioxetine
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Additional Strength/Form
  • 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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