欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DE/H/0480/001
药品名称Albunorm 5%
活性成分
    • albumin human 50.0 g/l
剂型Solution for infusion
上市许可持有人Octapharma GmbH Elisabeth-Selbert-Str. 11 D 40764 Langenfeld Germany
参考成员国 - 产品名称Germany (DE)
Albunorm 5%
互认成员国 - 产品名称
    • Denmark (DK)
    • Belgium (BE)
    • Netherlands (NL)
    • Luxembourg (LU)
    • Iceland (IS)
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
    • Austria (AT)
      Albunorm 50 g/l Infusionslösung
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Sweden (SE)
      Albunorm
    • Norway (NO)
    • Finland (FI)
    • Poland (PL)
      Albunorm 5%
    • Latvia (LV)
    • Lithuania (LT)
      Albunorm 50 g/l infuzinis tirpalas
    • Estonia (EE)
      ALBUNORM 50 G/L
    • Hungary (HU)
      ALBUNORM 50 g/l oldatos infúzió
    • Bulgaria (BG)
    • Cyprus (CY)
      albunorm 5% sol for infusion
    • Czechia (CZ)
    • Romania (RO)
      Albunorm 50 g/l, soluţie perfuzabilă
    • Slovakia (SK)
      Albunorm 5 %
    • Slovenia (SI)
    • Malta (MT)
许可日期2009/01/18
最近更新日期2024/04/19
药物ATC编码
    • B05AA01 albumin
申请类型
  • TypeLevel1：Known Active Substance
  • TypeLevel2：Initial Application
  • TypeLevel3：Bibliographic Art 10 a Dir 2001/83/EC
  • TypeLevel4：Biological: Blood Product
  • TypeLevel5：Prescription Only
附件文件下载
市场状态Positive
©2006-2024 Drugfuture->European Union HMA Authorisation of Medicines DataBase