欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号IE/H/0112/005
药品名称OxyContin Prolonged Release Tablets 5mg
活性成分
    • oxycodone hydrochloride 5.0 mg
剂型Prolonged-release tablet
上市许可持有人Napp Pharmaceuticals Limited Cambridge Science Park Milton Road Cambridge CB4 0GW United Kingdom
参考成员国 - 产品名称Ireland (IE)
互认成员国 - 产品名称
    • Austria (AT)
      OxyContin retard 5 mg Filmtabletten
    • Spain (ES)
    • Italy (IT)
许可日期2005/07/28
最近更新日期2024/06/11
药物ATC编码
    • N02AA05 oxycodone
申请类型
  • TypeLevel1:Line Extension
  • TypeLevel2:Initial Application
  • TypeLevel3:Full Dossier Article 4.8 Di 65/65
  • 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