欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号IE/H/1193/001
药品名称Plerixafor 20 mg/ml solution for injection
活性成分
    • PLERIXAFOR 20.0 mg/ml
剂型Solution for injection
上市许可持有人Seacross Pharma (Europe) Ltd, Regus Dublin Airport, Skybridge House, Corballis Road North, Dublin Airport Swords, Dublin, K67 P6K2, Ireland
参考成员国 - 产品名称Ireland (IE)
互认成员国 - 产品名称
    • Croatia (HR)
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
    • Poland (PL)
      Plerixafor Biofar
    • Lithuania (LT)
      Plerixafor Auxilia 20 mg/ml injekcinis tirpalas
    • Germany (DE)
      Plerixafor Seacross 20 mg/ml Injektionslösung
    • Estonia (EE)
    • Denmark (DK)
    • Hungary (HU)
    • Netherlands (NL)
      Plerixafor Seacross 20 mg/ml, oplossing voor injectie
    • Czechia (CZ)
      Plerixafor Onkogen
    • France (FR)
    • Romania (RO)
      Plerixafor Onkogen 20 mg/ml soluţie injectabilă
    • Spain (ES)
    • Slovakia (SK)
    • Portugal (PT)
    • Slovenia (SI)
    • Italy (IT)
许可日期2023/02/05
最近更新日期2023/10/20
药物ATC编码
    • L03AX16 plerixafor
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Generic Art 10.1 and 10.2 Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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