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
    • 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
    • Romania (RO)
      Duloxetină Sandoz 60 mg capsule gastrorezistente
许可日期2015/05/11
最近更新日期2024/11/15
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
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