欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号SK/H/0155/001
药品名称Dulsevia 30 mg hard gastro-resistant capsules
活性成分
    • Duloxetine 30.0 mg
剂型Gastro-resistant capsule, hard
上市许可持有人Krka, d.d., Novo mesto Šmarješka cesta 6 8501 Novo meto, Slovenia
参考成员国 - 产品名称Slovakia (SK)
Dulsevia 30 mg tvrdé gastrorezistentné kapsuly
互认成员国 - 产品名称
    • Greece (GR)
      DULOXENTA
    • Poland (PL)
      Dulsevia
    • Latvia (LV)
      Dulsevia 30 mg zarnās šķīstošās cietās kapsulas
    • Lithuania (LT)
      Dulsevia 30 mg skrandyje neirios kietosios kapsulės
    • Estonia (EE)
      DULSEVIA
    • Hungary (HU)
    • Bulgaria (BG)
      Dulsevia
    • Cyprus (CY)
      duloxenta 30 mg hard-resistant caps
    • Czechia (CZ)
      Duloxenta 30 mg
    • Romania (RO)
      DULSEVIA 30 mg capsule gastrorezistente
    • Slovenia (SI)
    • Croatia (HR)
      Dulsevia 30 mg tvrde želučanootporne kapsule
许可日期2015/03/27
最近更新日期2024/09/10
药物ATC编码
    • N06AX21 duloxetine
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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