欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号IE/V/0778/003
药品名称Clavusan tablets
活性成分
    • amoxicillin trihydrate 500.0 mg
    • clavulanic acid 125.0 mg
剂型Tablet
上市许可持有人Kuipersweg 9 3449 JA Woerden The Netherlands
参考成员国 - 产品名称Ireland (IE)
互认成员国 - 产品名称
    • Cyprus (CY)
    • Netherlands (NL)
    • Czechia (CZ)
    • Austria (AT)
    • Romania (RO)
    • Spain (ES)
    • Slovakia (SK)
    • Portugal (PT)
    • Slovenia (SI)
    • Italy (IT)
    • Croatia (HR)
    • Greece (GR)
    • Poland (PL)
    • Latvia (LV)
    • Lithuania (LT)
    • Denmark (DK)
    • Luxembourg (LU)
    • Estonia (EE)
    • Iceland (IS)
    • France (FR)
    • Hungary (HU)
    • Germany (DE)
    • Sweden (SE)
    • Norway (NO)
    • Bulgaria (BG)
    • Belgium (BE)
      Clavusan 500 mg + 125 mg
    • Finland (FI)
    • United Kingdom (Northern Ireland) (XI)
许可日期2023/02/08
最近更新日期2023/06/29
药物ATC编码
    • QJ01CR02 amoxicillin and beta-lactamase inhibitor
申请类型
  • TypeLevel1：non-food
  • TypeLevel2：Pharmaceutical
  • TypeLevel3：Other Generic application Art 13.3 Dir 2001/82/EC
  • TypeLevel4：[not specified]
  • TypeLevel5：[not specified]
附件文件下载
市场状态Positive
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