欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/1848/001
药品名称Vimovo
活性成分
    • esomeprazole magnesium salt 22.3 mg
    • naproxen 500.0 mg
剂型Modified-release tablet
上市许可持有人Grünenthal B.V. De Corridor 21k 3621 ZA Breukelen The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Vimovo 500 mg/20 mg, tablet met gereguleerde afgifte
互认成员国 - 产品名称
    • Germany (DE)
      Vimovo 500mg/20mg Tabletten mit modifizierter Wirkstofffreisetzung
    • United Kingdom (Northern Ireland) (XI)
    • Belgium (BE)
    • Luxembourg (LU)
    • Ireland (IE)
    • Austria (AT)
      Vimovo 500 mg/20 mg Tabletten mit veränderter Wirkstofffreisetzung
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
    • Lithuania (LT)
      Vimovo 500 mg/20 mg modifikuoto atpalaidavimo tabletės
    • Estonia (EE)
      VIMOVO
    • Bulgaria (BG)
      Vimovo
    • Romania (RO)
      VIMOVO 500 mg/20 mg comprimate cu eliberare modificată
许可日期2010/10/07
最近更新日期2024/04/25
药物ATC编码
    • M01AE52 naproxen and esomeprazole
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Fixed combination Art 10b 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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