欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号SE/H/1499/001
药品名称Bivalirudin Reig Jofre
活性成分
    • bivalirudin 250.0 mg
剂型Powder for concentrate for solution for infusion/injection
上市许可持有人Laboratorio Reig Jofre, S.A. Spain
参考成员国 - 产品名称Sweden (SE)
互认成员国 - 产品名称
    • Denmark (DK)
      55214
    • United Kingdom (Northern Ireland) (XI)
    • Spain (ES)
    • Finland (FI)
许可日期2015/11/19
最近更新日期2024/07/15
药物ATC编码
    • B01AE06 bivalirudin
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Initial Application
  • 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
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