欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号PT/H/0684/001
药品名称Augmentin ES
活性成分
    • amoxicillin trihydrate 600.0 mg/5ml
    • clavulanic acid 42.9 mg/5ml
剂型Powder for oral suspension
上市许可持有人GlaxoSmithkline Produtos Farmacêuticos, Lda.
参考成员国 - 产品名称Portugal (PT)
互认成员国 - 产品名称
    • Poland (PL)
      Augmentin ES
    • Bulgaria (BG)
    • Cyprus (CY)
    • Romania (RO)
      AUGMENTIN ES 600 mg/42,9 mg/ 5 ml pulbere pentru suspensie orală
    • Slovakia (SK)
      Augmentin ES
许可日期2011/03/25
最近更新日期2024/04/29
药物ATC编码
    • J01CR02 amoxicillin and beta-lactamase inhibitor
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Full Dossier Art 8.3(i) Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
附件文件下载
市场状态Positive
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