欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号PT/H/0992/004
药品名称Ceftriaxona Hospira
活性成分
    • ceftriaxone sodium salt 2.0 g
剂型Powder for solution for infusion/injection
上市许可持有人Hospira UK Limited
参考成员国 - 产品名称Portugal (PT)
Ceftriaxona Hospira
互认成员国 - 产品名称
    • Bulgaria (BG)
    • Malta (MT)
    • Netherlands (NL)
    • Poland (PL)
    • Romania (RO)
    • Lithuania (LT)
    • Latvia (LV)
    • Estonia (EE)
    • Slovenia (SI)
    • Belgium (BE)
      Ceftriaxone Hospira 2 g Poeder voor oplossing voor infusie
    • United Kingdom (Northern Ireland) (XI)
      Ceftriaxona Hospira
    • Italy (IT)
    • Cyprus (CY)
      CEFTRIAXONE HOSPIRA PWD FOR SOL FOR INJ/INF
    • Slovakia (SK)
许可日期2014/01/22
最近更新日期2018/12/11
药物ATC编码
    • J01DD04 ceftriaxone
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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