欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号IE/V/0541/001
药品名称Moxapulvis, 574 mg/g Powder for Use in Drinking Water
活性成分
    • amoxicillin trihydrate 574.0 mg/g
剂型Powder for use in drinking water
上市许可持有人VMD Livestock Pharma Hoge Mauw 900 2370 Arendonk Belgium
参考成员国 - 产品名称Ireland (IE)
互认成员国 - 产品名称
    • Belgium (BE)
      Moxapulvis 500 mg/g
    • Netherlands (NL)
    • Luxembourg (LU)
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Poland (PL)
    • Latvia (LV)
    • Lithuania (LT)
      MOXAPULVIS, 500 mg/g milteliai naudoti su geriamuoju vandeniu
    • Estonia (EE)
      Moxapulvis
    • Hungary (HU)
    • Bulgaria (BG)
    • Romania (RO)
    • Croatia (HR)
    • United Kingdom (Northern Ireland) (XI)
许可日期2018/10/30
最近更新日期2021/06/05
药物ATC编码
    • QJ01CA04 amoxicillin
申请类型
  • TypeLevel1:food
  • TypeLevel2:Pharmaceutical
  • TypeLevel3:Other Generic application Art 13.3 Dir 2001/82/EC
  • TypeLevel4:[not specified]
  • TypeLevel5:[not specified]
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市场状态Positive
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