欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号CZ/H/0503/001
药品名称Betaklav 500 mg/ 125 mg
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KRKA d.d. Novo Mesto Šmarješka cesta 6, 8501 Novo Mesto, Slovenia
参考成员国 - 产品名称Czechia (CZ)
BETAKLAV
互认成员国 - 产品名称
    • Denmark (DK)
    • Ireland (IE)
    • Austria (AT)
      Amoxicillin/Clavulansäure Krka 500 mg/125 mg Filmtabletten
    • Sweden (SE)
    • Finland (FI)
    • Poland (PL)
      Hiconcil combi
    • Latvia (LV)
      Betaklav 500 mg/125 mg apvalkotās tabletes
    • Lithuania (LT)
      Betaklav 500 mg / 125 mg plėvele dengtos tabletės
    • Estonia (EE)
      BETAKLAV
    • Hungary (HU)
      BETAKLAV 500 mg/125 mg filmtabletta
    • Bulgaria (BG)
      Betaklav
    • Slovakia (SK)
      Betaklav 500 mg/125 mg filmom obalené tablety
    • Slovenia (SI)
    • Croatia (HR)
      Betaklav 500 mg/125 mg filmom obložene tablete
许可日期2015/06/15
最近更新日期2024/01/12
药物ATC编码
    • J01CR02 amoxicillin and beta-lactamase inhibitor
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Generic Art 10.1 and 10.2 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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