欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/2215/001
药品名称Cefuroxime Pfizer 250 mg
活性成分
    • cefuroxime sodium salt 250.0 mg
剂型Powder for solution for infusion/injection
上市许可持有人Phizer bv Rivium Westlaan 142 2909 LD Caelle aan de IJssel The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Cefuroxim Pfizer 250 mg, poeder voor suspensie voor injectie of oplossing voor injectie
互认成员国 - 产品名称
    • Belgium (BE)
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
    • Denmark (DK)
    • France (FR)
    • Greece (GR)
许可日期2012/12/18
最近更新日期2024/08/19
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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