欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DE/H/0868/001
药品名称Ceftriaxon Kabi 1 g Pulver zur Herstellung einer Injektions-/Infusionslösung
活性成分
    • Ceftriaxone disodium salt hemiheptahydrate 1.19 g
剂型Powder for solution for injection/infusion
上市许可持有人Fresenius Kabi Deutschland GmbH Else-Kröner-Str. 1 61352 Bad Homburg Germany
参考成员国 - 产品名称Germany (DE)
互认成员国 - 产品名称
    • Iceland (IS)
    • Belgium (BE)
    • Netherlands (NL)
      Ceftriaxone Fresenius Kabi 1 g, poeder voor oplossing voor injectie
    • Austria (AT)
      Ceftriaxon Kabi 1 g Pulver zur Herstellung einer Infusionslösung
    • Greece (GR)
    • Finland (FI)
    • Poland (PL)
      Cefttiaxon Kabi 1 g
    • Hungary (HU)
      CEFTRIAXON KABI 1 g por oldatos injekcióhoz
    • Czechia (CZ)
    • Slovakia (SK)
      Ceftriaxon Kabi 1 g
    • Denmark (DK)
    • Luxembourg (LU)
    • Portugal (PT)
    • Sweden (SE)
    • Norway (NO)
    • Latvia (LV)
    • Lithuania (LT)
      Ceftriaxone Kabi 1 g milteliai injekciniam tirpalui
    • Estonia (EE)
      CEFTRIAXONE KABI 1 G
许可日期2007/08/28
最近更新日期2025/09/19
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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