欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DE/H/4238/002
药品名称Duloxetin - 1 A Pharma 60 mg magensaftresistente Hartkapseln
活性成分
    • duloxetine hydrochloride 33.66 mg
剂型Gastro-resistant capsule, hard
上市许可持有人1 A Pharma GmbH Industriestraße 18 83607 Holzkirchen Germany
参考成员国 - 产品名称Germany (DE)
Duloxetin - 1 A Pharma 60 mg magensaftresistente Hartkapsel
互认成员国 - 产品名称
    • Portugal (PT)
    • Denmark (DK)
      Duloxetine "Sandoz"
    • Luxembourg (LU)
    • United Kingdom (GB)
    • Estonia (EE)
    • Belgium (BE)
    • Netherlands (NL)
      Duloxetine Sandoz 60 mg, harde maagsapresistente capsules
    • United Kingdom (Northern Ireland) (XI)
    • Austria (AT)
    • France (FR)
    • Italy (IT)
    • Sweden (SE)
      Duloxetin - 1 A Pharma 60 mg magensaftresistente Hartkapsel
    • Ireland (IE)
    • Romania (RO)
      Duloxetină Sandoz 60 mg capsule gastrorezistente
    • Bulgaria (BG)
      Duloxetin Sandoz
    • Czechia (CZ)
      Duloxetin Sandoz 60 mg
    • Croatia (HR)
      Duloksetin Sandoz 60 mg tvrde želučanootporne kapsule
    • Lithuania (LT)
      Duloxetine Sandoz 60 mg skrandyje neirios kietosios kapsulės
许可日期2015/05/11
最近更新日期2024/04/16
药物ATC编码
    • N06AX21 duloxetine
申请类型
  • TypeLevel1：Abridged
  • TypeLevel2：Additional Strength/Form
  • 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
©2006-2024 Drugfuture->European Union HMA Authorisation of Medicines DataBase