欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号IE/H/0504/001
药品名称Duloxetine
活性成分
    • DULOXETINE HYDROCHLORIDE 30.0 mg
剂型Gastro-resistant capsule, hard
上市许可持有人Accord Healthcare Ireland Ltd., Euro House, Euro Business Park, Little Island, Cork T45 K857, Ireland Splitting of procedure - SE/H/1466/001-002 (old procedure number) to IE/H/504/001-002/DC (new procedure number)
参考成员国 - 产品名称Ireland (IE)
互认成员国 - 产品名称
    许可日期2017/07/25
    最近更新日期2023/08/10
    药物ATC编码
      • N06AX21 duloxetine
    申请类型
    • TypeLevel1:[not specified]
    • TypeLevel2:[not specified]
    • TypeLevel3:[not specified]
    • TypeLevel4:[not specified]
    • TypeLevel5:[not specified]
    附件文件下载
      市场状态Withdrawn(注:已撤市)
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