欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DK/H/2938/002
药品名称Sevelamer hydrochlorid
活性成分
    • sevelamer hydrochloride 800.0 mg
剂型Film-coated tablet
上市许可持有人Waymade BV Herikerbergweg 88 1101CM Amsterdam Netherlands
参考成员国 - 产品名称Denmark (DK)
Sevelamerhydrochlorid Waymade
互认成员国 - 产品名称
    • Germany (DE)
      Sevelamerhydrochlorid 800 mg Filmtabletten
    • Netherlands (NL)
      Sevelameerhydrochloride Waymade 800 mg, filmomhulde tabletten
    • Ireland (IE)
    • France (FR)
    • Spain (ES)
    • Italy (IT)
    • Greece (GR)
    • Romania (RO)
许可日期2019/08/15
最近更新日期2023/11/28
药物ATC编码
    • V03AE Drugs for treatment of hyperkalemia and hyperphosphatemia
    • V03AE02 sevelamer
申请类型
  • TypeLevel1：Known Active Substance
  • TypeLevel2：Additional Strength/Form
  • TypeLevel3：Other Generic application Art 10.3 Dir 2001/83/EC
  • TypeLevel4：Chemical Substance
  • TypeLevel5：Prescription Only
附件文件下载
市场状态Positive
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