欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号FI/H/1178/001
药品名称Cefuroxime Kalceks 750 mg
活性成分
    • cefuroxime sodium salt 750.0 mg
剂型Powder for solution for injection/infusion
上市许可持有人Kalceks AS Krustpils Iela 71e 1057 Riga Latvia
参考成员国 - 产品名称Finland (FI)
互认成员国 - 产品名称
    • Netherlands (NL)
    • Austria (AT)
    • France (FR)
    • Poland (PL)
    • Latvia (LV)
许可日期2023/09/19
最近更新日期2023/09/19
药物ATC编码
    • J01DC02 cefuroxime
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Initial Application
  • TypeLevel3:Generic Art 10.1 and 10.2 Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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