欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号FR/H/0290/001
药品名称Plasmion
活性成分
    • Sodium chloride 3.0 %
剂型Solution for infusion
上市许可持有人Fresenius Kabi France
参考成员国 - 产品名称France (FR)
互认成员国 - 产品名称
    • Hungary (HU)
      GELOPLASMA oldatos infúzió
    • Romania (RO)
    • Slovenia (SI)
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
    • Austria (AT)
      Geloplasma Infusionslösung
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Poland (PL)
      GELOPLASMA
    • Latvia (LV)
      Geloplasma solution for infusion
    • Lithuania (LT)
      GELOPLASMA infuzinis tirpalas
    • Estonia (EE)
      GELOPLASMA
    • Czechia (CZ)
      Geloplasma
    • Slovakia (SK)
      GELOPLASMA
许可日期2006/04/12
最近更新日期2025/02/13
药物ATC编码
    • A ALIMENTARY TRACT AND METABOLISM
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Biblio Art 10 a 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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