欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DK/H/0168/002
药品名称Trileptal
活性成分
    • Oxcarbazepine 300.0 mg
剂型Film-coated tablet
上市许可持有人Novartis Healthcare A/S Edvard Thomsens Vej 14 2300 Copenhagen Denmark
参考成员国 - 产品名称Denmark (DK)
Trileptal
互认成员国 - 产品名称
    • Spain (ES)
    • Croatia (HR)
    • Germany (DE)
      Trileptal
    • Belgium (BE)
      Trileptal
    • Netherlands (NL)
      Trileptal
    • Iceland (IS)
      Trileptal
    • Ireland (IE)
      Trileptal
    • Austria (AT)
      Trileptal 300 mg - Filmtabletten
    • France (FR)
      Trileptal
    • Greece (GR)
      Trileptal
    • Sweden (SE)
      Trileptal
    • Finland (FI)
      Trileptal
许可日期1999/11/30
最近更新日期2025/02/11
药物ATC编码
    • N03AF02 oxcarbazepine
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Positive
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