欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/5545/001
药品名称Azelastine/Fluticasonpropionaat CF 137 microgram/50 microgram per verstuiving, neusspray, suspensie
活性成分
    • azelastine hydrochloride 137.0 µg/actuation
    • fluticasone propionate 50.0 µg/actuation
剂型Nasal spray, suspension
上市许可持有人Centrafarm B.V. Van de Reijtstraat 31E 4814 NE Breda Netherlands
参考成员国 - 产品名称Netherlands (NL)
Azelastine/Fluticasonpropionaat CF 137 microgram/50 microgram per verstuiving, neusspray, suspensie
互认成员国 - 产品名称
    • Italy (IT)
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
      Azelastine hydrochloride/Fluticasone Stada
    • Poland (PL)
    • Hungary (HU)
      Azelastine/Fluticasone Stada 137 mikrogramm/50 mikrogramm szuszpenziós orrspray
    • Czechia (CZ)
      Zelatil
    • Slovakia (SK)
    • Germany (DE)
      Azelastin/Fluticason AL Nasenspray 137 Mikrogramm/50 Mikrogramm pro Sprühstoß Nasenspray, Suspension
    • Denmark (DK)
    • Ireland (IE)
    • France (FR)
许可日期2023/06/22
最近更新日期2023/06/23
药物ATC编码
    • R01AD58 fluticasone, combinations
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Initial Application
  • 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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