欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号IE/V/0652/003
药品名称Cladaxxa 500 mg chewable tablet
活性成分
    • amoxicillin trihydrate 45.92 mg
    • clavulanic acid 10.0 mg
    • potassium 23.84 mg
剂型Chewable tablet
上市许可持有人Krka Šmarješka cesta 6, 8501 Novo mesto
参考成员国 - 产品名称Ireland (IE)
Cladaxxa 500 mg chewable tablet
互认成员国 - 产品名称
    • Slovenia (SI)
    • Lithuania (LT)
    • Croatia (HR)
    • Latvia (LV)
    • United Kingdom (Northern Ireland) (XI)
    • Romania (RO)
    • Slovakia (SK)
    • Germany (DE)
    • Belgium (BE)
      Cladaxxa 400 mg/100 mg
    • Netherlands (NL)
    • France (FR)
    • Portugal (PT)
    • Italy (IT)
    • Estonia (EE)
    • Poland (PL)
    • Hungary (HU)
    • Czechia (CZ)
      Cladaxxa 400 mg/100 mg žvýkací tablety pro psy
许可日期2021/04/28
最近更新日期2023/11/11
药物ATC编码
    • QJ01CR02 amoxicillin and beta-lactamase inhibitor
申请类型
  • TypeLevel1:non-food
  • TypeLevel2:Pharmaceutical
  • TypeLevel3:Generic - art 13.2 Dir 2001/82/EC
  • TypeLevel4:[not specified]
  • TypeLevel5:[not specified]
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市场状态Positive
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