欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号PT/V/0101/001
药品名称CEFTIOMAX 50 mg/ml ceftiofur suspension for injection for swine and cattle
活性成分
    • ceftiofur hydrochloride 50.0 mg/ml
剂型Suspension for injection
上市许可持有人CALIER PORTUGAL, S.A.
参考成员国 - 产品名称Portugal (PT)
互认成员国 - 产品名称
    • Poland (PL)
      Ceftiomax 50 mg/ml suspension for injection for swine and cattle
    • Hungary (HU)
    • Czechia (CZ)
    • Germany (DE)
    • Belgium (BE)
      Readycef 50 mg/ml
    • Netherlands (NL)
    • United Kingdom (Northern Ireland) (XI)
    • Austria (AT)
    • France (FR)
      READYCEF 50 MG/ML SUSPENSION INJECTABLE POUR PORCINS ET BOVINS
    • Spain (ES)
    • Italy (IT)
    • Greece (GR)
    • Latvia (LV)
    • Lithuania (LT)
    • Estonia (EE)
    • Bulgaria (BG)
    • Romania (RO)
    • Slovakia (SK)
许可日期2008/04/18
最近更新日期2019/10/12
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
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