欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/4762/002
药品名称Cefuroxim Fresenius Kabi 1500 mg, poeder voor oplossing voor injectie/infusie
活性成分
    • cefuroxime 1500.0 mg
剂型Powder for solution for injection
上市许可持有人Fresenius Kabi Nederland B.V. Amersfoortseweg 10E 3712 BC Huis ter Heide Nederland
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    • Denmark (DK)
      Cefuroxime Yes
    • Belgium (BE)
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
    • Greece (GR)
    • Norway (NO)
    • Poland (PL)
    • Hungary (HU)
      CEFUROXIM KABI 1500 mg por oldatos injekcióhoz
    • Czechia (CZ)
      Cefuroxim YES 1,5 g
    • Slovakia (SK)
      Cefuroxim YES 1500 mg
    • Iceland (IS)
许可日期2008/11/27
最近更新日期2023/09/22
药物ATC编码
    • J01DC02 cefuroxime
申请类型
  • TypeLevel1:[not specified]
  • TypeLevel2:[not specified]
  • TypeLevel3:[not specified]
  • TypeLevel4:[not specified]
  • TypeLevel5:[not specified]
附件文件下载
市场状态Positive
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