欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/5318/004
药品名称Lenalidomide Alkaloid-INT 25 mg
活性成分
    • lenalidomide 25.0 mg
剂型Capsule, hard
上市许可持有人ALKALOID – INT d.o.o Šlandrova ulica 4, 1231 Ljubljana-Črnuče Slovenia
参考成员国 - 产品名称Netherlands (NL)
Lenalidomide Alkaloid-INT 25 mg, harde capsules
互认成员国 - 产品名称
    • Bulgaria (BG)
      Lenalidomide Alkaloid
    • Romania (RO)
      Lenalidomidă Alkaloid-INT 25 mg capsule
    • Slovenia (SI)
    • Croatia (HR)
      Lenalidomid Alkaloid-INT 25 mg tvrde kapsule
许可日期2021/02/03
最近更新日期2024/07/25
药物ATC编码
    • L04AX04 lenalidomide
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
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