欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/V/0186/001
药品名称Amoxibactin 50 mg tablets for dogs and cats
活性成分
    • amoxicillin trihydrate 50.0 mg
剂型Tablet
上市许可持有人Le Vet Beheer B.V. Wilgenweg 7 3421 TV Oudewater The Netherlands
参考成员国 - 产品名称Netherlands (NL)
AMOXIBACTIN 50 mg, palatable tablets for dogs and cats
互认成员国 - 产品名称
    • Germany (DE)
    • Sweden (SE)
    • Denmark (DK)
      Amoxibactin Vet.
    • Belgium (BE)
      Amoxibactin 50 mg
    • Luxembourg (LU)
    • Iceland (IS)
      Amoxibactin vet 50 mg Tafla handa hundum og köttum
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
      Amoxibactin 50mg, 250mg & 500mg Palatable Tablets for dogs and cats
    • Austria (AT)
      Amoxibactin 50 mg Tabletten für Hunde und Katzen
    • France (FR)
      AMOXIBACTIN 50 MG COMPRIMES POUR CHIENS ET CHATS (13712)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Norway (NO)
      Amoxibactin vet
    • Finland (FI)
    • Poland (PL)
    • Latvia (LV)
      Amoxibactin
    • Lithuania (LT)
    • Estonia (EE)
      Amoxibactin vet
    • Hungary (HU)
    • Cyprus (CY)
    • Czechia (CZ)
      Amoxibactin 50 mg tablety pro psy a kočky
    • Romania (RO)
    • Slovakia (SK)
许可日期2014/09/24
最近更新日期2022/07/27
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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