欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号IT/H/0790/002
药品名称AIRSUS
活性成分
    • fluticasone propionate 125.0 mcg
    • salmeterol xinafoate 25.0 mcg
剂型Pressurised inhalation, suspension
上市许可持有人Genetic S.p.A, Via Della Monica 26, 84083 Castel San Giorgio (SA), Italy
参考成员国 - 产品名称Italy (IT)
互认成员国 - 产品名称
    • United Kingdom (Northern Ireland) (XI)
    • Greece (GR)
      SALMETEROL+FLUTICASONE/GENETIC SPA
    • Poland (PL)
      Fluticomb
许可日期2017/10/16
最近更新日期2023/06/20
药物ATC编码
    • R03AK06 salmeterol and fluticasone
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
©2006-2024 Drugfuture->European Union HMA Authorisation of Medicines DataBase