欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/4563/001
药品名称Fludarabine 25 mg/ml Concentrate for Solution for Injection or Infusion
活性成分
    • Fludarabine 25.0 mg/ml
剂型Solution for injection/infusion
上市许可持有人Accord Healthcare Ltd Sage House, 319 Pinner Road HA1 4HF North Harrow, Middlesex United Kingdom
参考成员国 - 产品名称Netherlands (NL)
Fludarabinefosfaat Accord 25 mg/ml, concentraat voor oplossing voor injectie of infusie
互认成员国 - 产品名称
    • Romania (RO)
      Fludarabină Accord 25 mg/ml concentrat pentru soluție injectabilă sau perfuzabilă
    • Slovenia (SI)
    • Poland (PL)
      Fludarabine Accord
    • Czechia (CZ)
      Fludarabine Accord 25 mg/ml Koncentrát pro přípravu injekčního nebo infuzního roztoku
    • Croatia (HR)
    • United Kingdom (Northern Ireland) (XI)
      Fludarabine 25 mg/ml Concentrate for Solution for Injection or Infusion
    • Germany (DE)
      Fludarabin Accord 25 mg7ml Konzentrat zur Herstellung einer Injektions- oder Infusionslösung
    • Belgium (BE)
      Fludarabine Accord Healthcare 25 mg/ml concentraat voor oplossing voor injectie of infusie
    • Ireland (IE)
    • Austria (AT)
      Fludarabin Accord 25 mg/ml Konzentrat zur Herstellung einer Injektions- oder Infusionslösung
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Sweden (SE)
    • Finland (FI)
    • Lithuania (LT)
      Fludarabine Accord 25 mg/ml koncentratas injekciniam ar infuziniam tirpalui
    • Estonia (EE)
      FLUDARABINE ACCORD 25 MG/ML
    • Hungary (HU)
      FLUDARABIN ACCORD 25 mg/ml koncentrátum oldatos injekcióhoz vagy infúzióhoz
    • Bulgaria (BG)
      Fludarabine Accord
    • Cyprus (CY)
      FLUDARABINE ACCORD CON FOR SOL FOR INJ/INF
许可日期2014/08/11
最近更新日期2024/11/25
药物ATC编码
    • L01BB05 fludarabine
申请类型
  • TypeLevel1:[not specified]
  • TypeLevel2:[not specified]
  • TypeLevel3:[not specified]
  • TypeLevel4:[not specified]
  • TypeLevel5:[not specified]
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市场状态Positive
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