欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号PT/H/0985/004
药品名称Amoxicilina + Ácido Clavulânico Kabi
活性成分
    • amoxicillin sodium salt 2000.0 mg
    • clavulanic acid potassium salt 200.0 mg
剂型Powder for solution for injection
上市许可持有人Fresenius Kabi Pharma Portugal, Lda.
参考成员国 - 产品名称Portugal (PT)
互认成员国 - 产品名称
    • Germany (DE)
      Amoicillin/Clavulanic acid Kabi 2000 mg/200mg Pulver zur Herstellung einer Infusionslösung
    • Belgium (BE)
      Amoxiclav Fresenius Kabi 2000 mg/200 mg poeder voor oplossing voor infusie
    • Netherlands (NL)
    • Luxembourg (LU)
    • France (FR)
    • Spain (ES)
    • Italy (IT)
    • Poland (PL)
      Amoxicillin/Clavuclanic Acid Kabi
    • Hungary (HU)
      AMOXICILLIN/KLAVULÁNSAV KABI 2000 mg/200 mg por oldatos infúzióhoz
许可日期2014/01/09
最近更新日期2024/04/02
药物ATC编码
    • J01CR02 amoxicillin and beta-lactamase inhibitor
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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