欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/5646/001
药品名称Fluticasonfuroaat Teva 27,5 microgram/dosis, neusspray suspensie
活性成分
    • Fluticasone furoate 27.5 µg/dose
剂型Nasal spray, suspension
上市许可持有人Teva B.V. Swensweg 5 2031 GA Netherlands
参考成员国 - 产品名称Netherlands (NL)
Fluticasonfuroaat Teva 27,5 microgram/dosis, neusspray suspensie
互认成员国 - 产品名称
    • Ireland (IE)
    • France (FR)
    • Portugal (PT)
    • Finland (FI)
    • Poland (PL)
      Fluticasone furoate Teva
    • Latvia (LV)
    • Estonia (EE)
    • Czechia (CZ)
      Fluticasone Teva
    • Denmark (DK)
      Fluticasonfuroat Teva
    • Iceland (IS)
许可日期2024/04/02
最近更新日期2024/11/18
药物ATC编码
    • R01AD12 fluticasone furoate
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
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市场状态Positive
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