欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号IE/V/0303/001
药品名称Ceftiokel 50 mg/ml, suspension for Injection
活性成分
    • CEFTIOFUR 50.0 mg
剂型Suspension for injection
上市许可持有人KELA N.V. St. Lenaartseweg 48 2320 Hoogstraten Belgium
参考成员国 - 产品名称Ireland (IE)
Cefokel 50mg/ml, suspension for injection for pigs and cattle
互认成员国 - 产品名称
    • Germany (DE)
      Ceftiokel
    • Belgium (BE)
      Cefokel 50 mg/ml
    • Luxembourg (LU)
    • United Kingdom (Northern Ireland) (XI)
    • Poland (PL)
      Cefokel 50 mg/ml, suspension for injection for pigs and cattle
    • Romania (RO)
许可日期2013/03/20
最近更新日期2025/09/16
药物ATC编码
    • QJ01DD90 ceftiofur
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
©2006-2025 Drugfuture->European Union HMA Authorisation of Medicines DataBase