欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号PT/H/1334/002
药品名称Duloxetina Aurobindo
活性成分
    • duloxetine 30.0 mg
剂型Gastro-resistant capsule, hard
上市许可持有人Aurobindo Pharma (Portugal), Unipessoal, Lda.
参考成员国 - 产品名称Portugal (PT)
互认成员国 - 产品名称
    • Germany (DE)
      Duloxetin Aurobindo 30 mg magensaftresistente Hartkapseln
    • Belgium (BE)
      Duloxetine AB 30mg maagsapresistente capsules, hard
    • Netherlands (NL)
      Duloxetine Aurobindo 30 mg, harde maagsapresistente capsules
    • Italy (IT)
许可日期2015/07/08
最近更新日期2024/03/07
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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