欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/3288/001
药品名称Duloxetine Accord 30 mg harde maagsapresistente capsules
活性成分
    • duloxetine hydrochloride 30.0 mg
剂型Gastro-resistant capsule, hard
上市许可持有人Accord Healthcare B.V. Winthontlaan 200 3508 AD Utrecht Netherlands
参考成员国 - 产品名称Netherlands (NL)
Duloxetine Accord 30 mg harde maagsapresistente capsules
互认成员国 - 产品名称
    • Denmark (DK)
    • United Kingdom (Northern Ireland) (XI)
    • Austria (AT)
      Duloxetin Accord 30 mg magensaftresistente Hartkapseln
    • France (FR)
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
    • Cyprus (CY)
许可日期2015/09/09
最近更新日期2024/04/02
药物ATC编码
    • N06AX21 duloxetine
申请类型
  • TypeLevel1：Known Active Substance
  • TypeLevel2：Multiple (Copy) 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
©2006-2024 Drugfuture->European Union HMA Authorisation of Medicines DataBase