欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号SK/H/0155/003
药品名称Dulsevia 90 mg hard gastro-resistant capsules
活性成分
    • Duloxetine hydrochloride 90.0 mg
剂型Gastro-resistant capsule, hard
上市许可持有人KRKA, d.d., Novo mesto Šmarješka cesta 6 8501 Novo mesto, Slovenia
参考成员国 - 产品名称Slovakia (SK)
Dulsevia 90 mg tvrdé gastrorezistentné kapsuly
互认成员国 - 产品名称
    • Poland (PL)
      Dulsevia
    • Estonia (EE)
      DULSEVIA
    • Hungary (HU)
    • Bulgaria (BG)
      Dulsevia
    • Romania (RO)
      DULSEVIA 90 mg capsule gastrorezistente
    • Slovenia (SI)
      Dulsevia 90 mg trde gastrorezistentne kapsule
    • Croatia (HR)
      Dulsevia 90 mg tvrde želučanootporne kapsule
    • Czechia (CZ)
许可日期2017/07/25
最近更新日期2024/09/10
药物ATC编码
    • N06AX21 duloxetine
申请类型
  • TypeLevel1:Line Extension
  • TypeLevel2:Additional Strength/Form
  • 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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