欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/6032/001
药品名称Augmentan 500 mg/125 mg Filmtabletten
活性成分
    • amoxicillin 500.0 mg
    • clavulanic acid 125.0 mg
剂型Film-coated tablet
上市许可持有人GlaxoSmithKline GmbH & Co. KG Prinzregentenplatz 9 81675 München Germany
参考成员国 - 产品名称Germany (DE)
Augmentan 500 mg/125 mg Filmtabletten
互认成员国 - 产品名称
    • Portugal (PT)
    • Spain (ES)
    • Norway (NO)
    • Belgium (BE)
    • Netherlands (NL)
    • Luxembourg (LU)
    • Ireland (IE)
    • Austria (AT)
    • Greece (GR)
    • Poland (PL)
      Augmentin
    • Latvia (LV)
    • Lithuania (LT)
      Augmentin 500 mg /125 mg plėvele dengtos tabletės
    • Hungary (HU)
      AUGMENTIN 500 mg/125 mg filmtabletta
    • Bulgaria (BG)
    • Cyprus (CY)
    • Czechia (CZ)
    • Romania (RO)
      Augmentin 500 mg/125 mg comprimate filmate
    • Slovakia (SK)
      Augmentin 625 mg
    • Malta (MT)
    • United Kingdom (Northern Ireland) (XI)
      PL 00038/0362 - 0117
许可日期2012/06/13
最近更新日期2024/03/15
药物ATC编码
    • J01CR02 amoxicillin and beta-lactamase inhibitor
申请类型
  • TypeLevel1:[not specified]
  • TypeLevel2:[not specified]
  • TypeLevel3:[not specified]
  • TypeLevel4:[not specified]
  • TypeLevel5:[not specified]
附件文件下载
市场状态Positive
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