欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号IE/V/0325/001
药品名称Maxyl 50% w/w POWDER FOR ORAL SOLUTION
活性成分
    • amoxicillin trihydrate 50.0 %
剂型Powder for oral solution
上市许可持有人Vetpharma Animal Health S.L
参考成员国 - 产品名称Ireland (IE)
MAXYL 500 mg/g Powder for use in drinking water for chickens, turkeys, ducks and pigs
互认成员国 - 产品名称
    • Slovenia (SI)
    • Germany (DE)
      Maxyl
    • Denmark (DK)
      Maxyl
    • Netherlands (NL)
    • United Kingdom (Northern Ireland) (XI)
    • Austria (AT)
      Maxyl, 500 mg/g, Pulver zum Eingeben über das Trinkwasser für Hühner, Puten, Enten und Schweine
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Sweden (SE)
      49680
    • Poland (PL)
    • Hungary (HU)
    • Cyprus (CY)
许可日期2014/06/18
最近更新日期2021/05/26
药物ATC编码
    • QJ01CA04 amoxicillin
申请类型
  • TypeLevel1:[not specified]
  • TypeLevel2:[not specified]
  • TypeLevel3:Generic - art 13.2 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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