欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/1147/001
药品名称Phoxilium
活性成分
    • calcium chloride dihydrate 3.68 g
    • magnesium chloride hexahydrate 2.44 g
剂型Solution for haemofiltration
上市许可持有人GAMBRO Lundia AB Magistratsvägen 16 S-22010 Lund Sweden
参考成员国 - 产品名称Netherlands (NL)
Phoxilium 1,2 mmol/l fosfaat oplossing voor hemodialyse/hemofiltratie
互认成员国 - 产品名称
    • Germany (DE)
    • Denmark (DK)
    • 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)
    • Romania (RO)
    • Slovakia (SK)
    • Slovenia (SI)
    • Malta (MT)
    • United Kingdom (Northern Ireland) (XI)
    • Belgium (BE)
许可日期2009/02/05
最近更新日期2024/01/12
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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