欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/1707/002
药品名称Amoxicillin/Clavulanic acid Aurobindo 875/125 mg
活性成分
    • amoxicillin trihydrate 875.0 mg
    • clavulanic acid potassium salt 125.0 mg
剂型Film-coated tablet
上市许可持有人Aurobindo Pharma B.V. Baarnsche Dijk 1 3741 LN Baarn Netherlands
参考成员国 - 产品名称Netherlands (NL)
Amoxicilline/Clavulaanzuur Aurobindo 875 mg/125 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Germany (DE)
      Amoxi-Clavulan Aurobindo 875 mg/ 125 mg Filmtabletten
    • Austria (AT)
      Amoxicillin/Clavulansäure Aurobindo 875 mg/125 mg Filmtabletten
    • Spain (ES)
    • Italy (IT)
    • Sweden (SE)
      Amoxicillin/Clavulanic acid Aurobindo
    • Romania (RO)
      Amoxicilină / Acid clavulanic Aurobindo 875 mg/125 mg comprimate filmate
    • Denmark (DK)
许可日期2009/09/22
最近更新日期2023/09/08
药物ATC编码
    • J01CR02 amoxicillin and beta-lactamase inhibitor
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Additional Strength/Form
  • TypeLevel3:Generic Art 10.1 and 10.2 Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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