欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/4910/001
药品名称Travoprost + Timolol/RAFARM 40 micrograms/mL + 5 mg/mL
活性成分
    • timolol 5.0 mg/ml
    • travoprost 40.0 µg/ml
剂型Eye drops, solution
上市许可持有人Rafarm S.A.
参考成员国 - 产品名称Netherlands (NL)
Travoprost + Timolol/RAFARM 40 μg/mL + 5 mg/mL oogdruppels, oplossing
互认成员国 - 产品名称
    • Cyprus (CY)
      Travoprost/Timolol Rafarm 40mcg/5mg/ml
    • France (FR)
    • Germany (DE)
      Travoprost + Timolol/RAFARM 40 µg/ml + 5 mg/ml Augentropfen, Lösung
    • Greece (GR)
    • Italy (IT)
    • Spain (ES)
许可日期2021/02/24
最近更新日期2021/12/10
药物ATC编码
    • S01ED51 timolol, combinations
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
附件文件下载
    市场状态Withdrawn(注:已撤市)
    ©2006-2025 Drugfuture->European Union HMA Authorisation of Medicines DataBase