欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/0504/001
药品名称Duosol zonder Kalium, oplossing voor haemofiltratie
活性成分
    • calcium chloride anhydrous dihydrate 0.22 mg/ml
    • glucose monohydrate 1.1 mg/ml
    • magnesium chloride hexahydrate 0.1 mg/ml
    • sodium bicarbonate 3.19 mg/ml
    • sodium chloride 5.96 mg/ml
剂型Solution for haemofiltration
上市许可持有人B.Braun Avitum AG Schwarzenberger Weg 73-79 D-34212 Melsungen Germany
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    • Germany (DE)
      Duosol K0
    • Luxembourg (LU)
    • Italy (IT)
    • Finland (FI)
      Duosol sine kalium, hemofiltraationeste
    • Czechia (CZ)
      Duosol bez kalia
    • United Kingdom (Northern Ireland) (XI)
    • Spain (ES)
      PRIOSOL SIN POTASIO solución para hemofiltración
    • Poland (PL)
      Duosol roztwor nie zawierajacy potasu
    • Latvia (LV)
      Duosol bez kālija
    • Lithuania (LT)
      Duosol K O hemofiltracijos tirpalas
    • Estonia (EE)
    • Slovenia (SI)
    • Denmark (DK)
    • Ireland (IE)
    • Austria (AT)
    • France (FR)
    • Portugal (PT)
    • Greece (GR)
    • Sweden (SE)
    • Norway (NO)
    • Bulgaria (BG)
      Duosol without potassium
    • Romania (RO)
      Nefrosol fără potasiu soluție pentru hemofiltrare
    • Croatia (HR)
      Duosol bez kalija otopina za hemofiltraciju
许可日期2004/09/19
最近更新日期2024/03/22
药物ATC编码
    • B05ZB Hemofiltrates
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Bibliographic Article 4.8 (a) (ii)
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
附件文件下载
市场状态Positive
©2006-2024 Drugfuture->European Union HMA Authorisation of Medicines DataBase