欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/4174/001
药品名称Dutilox 30 mg magensaftresistente Hartkapseln
活性成分
    • Duloxetine hydrochloride 33.68 mg
剂型Gastro-resistant capsule, hard
上市许可持有人Towa Pharmaceutical Europe S.L. Carrer de Sant Marti 75-97 ES-08107 Martorelles, Barcelona Spain
参考成员国 - 产品名称Germany (DE)
Dutilox 30 mg magensaftresistente Hartkapsel
互认成员国 - 产品名称
    • Ireland (IE)
    • Belgium (BE)
      Dutilox 30 mg harde maagsapresistente capsules
    • Netherlands (NL)
      Dutilox 30 mg harde maagsapresistente capsules
    • Austria (AT)
      Dutilox 30 mg magensaftresistente Hartkapseln
    • Poland (PL)
      Dutilox
    • Romania (RO)
      Dutilox 30 mg capsule gastrorezistente
许可日期2015/04/28
最近更新日期2024/11/04
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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