欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/4286/004
药品名称Lenalidomide Grindeks 10 mg
活性成分
    • lenalidomide 10.0 mg
剂型Capsule, hard
上市许可持有人AS Grindeks Krustpils Iela 53, LV-1057,Riga,Latvia
参考成员国 - 产品名称Netherlands (NL)
Lenalidomide Grindeks 10 mg harde capsules
互认成员国 - 产品名称
    • Norway (NO)
    • Denmark (DK)
      Lenalidomid ”Grindeks”
    • Ireland (IE)
    • Iceland (IS)
    • Portugal (PT)
    • Germany (DE)
      Lenalidomide Grindeks 10 mg Hartkapseln
    • Italy (IT)
    • Sweden (SE)
    • Poland (PL)
    • Latvia (LV)
      Lenalidomide Grindeks 10 mg cietās kapsulas
    • Lithuania (LT)
      Lenalidomide Grindeks 10 mg kietosios kapsulės
    • Estonia (EE)
      LENALIDOMIDE GRINDEKS
    • Hungary (HU)
      LENALIDOMIDE GRINDEKS 10 mg kemény kapszula
    • Bulgaria (BG)
      Lenalidomide Grindex
    • Czechia (CZ)
      Lenalidomide Grindeks
    • Romania (RO)
      Lenalidomide Grindeks 10 mg, capsule, tari
    • Slovakia (SK)
      Lenalidomid Grindeks 10 mg tvrdé kapsuly
    • Slovenia (SI)
    • Greece (GR)
    • Croatia (HR)
      Lenalidomid Grindeks 10 mg tvrde kapsule
    • Austria (AT)
    • Spain (ES)
    • Finland (FI)
    • United Kingdom (Northern Ireland) (XI)
    • Belgium (BE)
    • Malta (MT)
    • France (FR)
    • Cyprus (CY)
      Lenalidomide Grindeks 10 mg capsule, hard
许可日期2019/08/21
最近更新日期2024/09/23
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
©2006-2025 Drugfuture->European Union HMA Authorisation of Medicines DataBase