欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号IE/H/0434/002
药品名称Fluticasone
活性成分
    • fluticasone propionate 250.0 µg
剂型Pressurised inhalation, suspension
上市许可持有人Momaja s.r.o
参考成员国 - 产品名称Ireland (IE)
Fluticasone Momaja 125/250 microgram per actuation Pressurized
互认成员国 - 产品名称
    • Poland (PL)
      Efletua
    • Bulgaria (BG)
      Fluticasone Momaja
    • Romania (RO)
      Arquist 250 micrograme suspensie de inhalat presurizată
    • Croatia (HR)
      Truflo 250 mikrograma/dozi, stlačeni inhalat, suspenzija
许可日期2015/04/23
最近更新日期2024/04/05
药物ATC编码
    • R03BA05 fluticasone
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Other Generic application Art 10.3 Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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    市场状态Positive
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