欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号MT/H/0325/001
药品名称Dutasteride/Tamsulosin Sandoz 0.5 mg/0.4 mg hard capsules
活性成分
    • Dutasteride 0.5 mg
    • Tamsulosin hydrochloride 0.4 mg
剂型Capsule, hard
上市许可持有人Sandoz pharmaceuticals d.d., Verovškova ulica 57, SI-1000 Ljubljana (Slovenia) ex Galenicum Health SL Avda. Diagonal 123,planta 11 08005 BArcelona (Spain)
参考成员国 - 产品名称Malta (MT)
Dutasteride/Tamsulosin Adair 0.5mg/0.4mg hard capsules
互认成员国 - 产品名称
    • France (FR)
    • Belgium (BE)
      Dutasteride/Tamsulosine Sandoz 0,5 mg/0,4 mg harde capsules
    • Bulgaria (BG)
      Tamprost Combi
    • Czechia (CZ)
      Dutasteride/Tamsulosin Sandoz
    • Germany (DE)
      Dutacomp - 1 A Pharma 0,5 mg/0,4 mg Hartkapseln
    • Finland (FI)
    • Lithuania (LT)
    • Netherlands (NL)
      Dutasteride/Tamsulosine HCL Sandoz 0,5 mg/0,4 mg, harde capsules
    • Slovenia (SI)
    • Spain (ES)
    • Norway (NO)
      Dutasteride/Tamsulosin Hexal
许可日期2019/08/09
最近更新日期2025/02/03
药物ATC编码
    • G04CA52 tamsulosin and dutasteride
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Multiple (Copy) 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
©2006-2025 Drugfuture->European Union HMA Authorisation of Medicines DataBase