欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/5969/003
药品名称Brivaracetam Teva 50 mg
活性成分
    • Brivaracetam 50.0 mg
剂型Film-coated tablet
上市许可持有人Teva B.V. Swensweg 5 2031GA Haarlem Netherlands
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    • Luxembourg (LU)
    • France (FR)
    • Spain (ES)
    • Italy (IT)
    • Sweden (SE)
    • Finland (FI)
    • Poland (PL)
    • Hungary (HU)
    • Czechia (CZ)
      Brivaracetam Teva
    • Germany (DE)
      Brivaracetam-ratiopharm 50 mg Filmtabletten
    • Romania (RO)
    • Denmark (DK)
      Brivaracetam ”Teva”
    • Slovakia (SK)
    • Belgium (BE)
      Brivaracetam Teva 50 mg filmomhulde tabletten
许可日期2025/03/11
最近更新日期2025/05/08
药物ATC编码
    • N03AX23 brivaracetam
申请类型
  • TypeLevel1：Abridged
  • 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Positive
    ©2006-2025 Drugfuture->European Union HMA Authorisation of Medicines DataBase