欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号CZ/H/0570/007
药品名称Prabegin 225 mg
活性成分
    • pregabalin 225.0 mg
剂型Capsule, hard
上市许可持有人Egis Pharmaceuticals PLC Keresztúri út 30-38 H-1106 Budapest
参考成员国 - 产品名称Czechia (CZ)
Prabegin 225 mg
互认成员国 - 产品名称
    • Bulgaria (BG)
      Prabegin
    • Croatia (HR)
    • Hungary (HU)
    • Poland (PL)
      Prabegin
    • Romania (RO)
    • Slovenia (SI)
    • Slovakia (SK)
      Prabegin 225 mg
许可日期2016/01/27
最近更新日期2016/10/18
药物ATC编码
    • N03AX16 pregabalin
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Additional Strength/Form
  • 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Withdrawn(注:已撤市)
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