欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号IE/H/0157/001
药品名称Lipantil Supra 215 mg, film-coated tablet.
活性成分
    • fenofibrate 215.0 mg
剂型Film-coated tablet
上市许可持有人Mylan IRE Healthcare Limited, Unit 35/36, Grange Parade, Baldoyle Industrial Estate, Dublin 13, Ireland
参考成员国 - 产品名称Ireland (IE)
互认成员国 - 产品名称
    • Poland (PL)
    • Czechia (CZ)
    • Slovakia (SK)
许可日期2005/07/10
最近更新日期2024/03/04
药物ATC编码
    • C10AB05 fenofibrate
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Full Dossier [Article 8.3(i)]
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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