欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DK/H/1948/001
药品名称Sevelamercarbonat "Synthon"
活性成分
    • sevelamer carbonate 800.0 mg
剂型Film-coated tablet
上市许可持有人Synthon BV Microweg 22 6545 CM, Nijmegen The Netherlands
参考成员国 - 产品名称Denmark (DK)
Sevelamercarbonat "Synthon"
互认成员国 - 产品名称
    • Iceland (IS)
    • Greece (GR)
      SEVELAMER/PROTON
    • Finland (FI)
    • Poland (PL)
      Sewelameru węglan Synthon
    • Latvia (LV)
    • Lithuania (LT)
      Sevelamer Synthon 800 mg plėvele dengtos tabletės
    • Estonia (EE)
      Sevelamer Auxilia
    • Hungary (HU)
      Szevelamer-Karbonát Synthon 800 mg ftbl.
    • Cyprus (CY)
      Sevelamer Ledpharm 800mg film-coated tablets
许可日期2014/03/12
最近更新日期2023/06/27
药物ATC编码
    • V03AE02 sevelamer
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Initial Application
  • TypeLevel3:Other Generic application Art 10.3 Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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