欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/3002/001
药品名称Biphozyl 22 mmol/l
活性成分
    • magnesium chloride hexahydrate 3.05 g/l
    • potassium chloride 0.31 g/l
    • sodium chloride 7.01 g/l
    • sodium carbonate 2.12 g/l
    • SODIUM PHOSPHATE DIBASIC dihydrate 0.19 g/l
剂型Solution for haemodialysis/haemofiltration
上市许可持有人Baxter Holding B.V., Kobaltweg 49, 3542CE Utrecht, The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Biphozyl 22 mmol/l, oplossing voor hemofiltratie en hemodialys
互认成员国 - 产品名称
    • Germany (DE)
    • Denmark (DK)
    • Belgium (BE)
    • Luxembourg (LU)
    • Iceland (IS)
    • Ireland (IE)
    • Austria (AT)
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
    • Poland (PL)
    • Latvia (LV)
    • Lithuania (LT)
    • Estonia (EE)
    • Hungary (HU)
    • Bulgaria (BG)
    • Cyprus (CY)
    • Czechia (CZ)
    • Romania (RO)
    • Slovakia (SK)
    • Slovenia (SI)
    • Malta (MT)
    • Croatia (HR)
    • United Kingdom (Northern Ireland) (XI)
许可日期2014/10/20
最近更新日期2023/09/06
药物ATC编码
    • B05ZB Hemofiltrates
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Bibliographic Art 10 a Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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