欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Naxcel
适用类别Veterinary
治疗领域
通用名/非专利名称ceftiofur
活性成分ceftiofur
产品号EMEA/V/C/000079
患者安全信息no
授权状态Authorised
ATC编码
是否额外监管no
是否仿制药no
是否生物类似药no
是否附条件批准no
是否特殊情形no
是否加速审评no
是否罕用药no
批准上市日期2005/05/19
上市许可持有人/公司名称Zoetis Belgium SA
兽用药物治疗分组Antibacterials for systemic use
审评意见发布日期2005/05/11
决定日期2020/07/17
修订号15
适应症PigsTreatment of bacterial respiratory disease associated with Actinobacillus pleuropneumoniae, Pasteurella multocida, Haemophilus parasuis and Streptococcus suis.Treatment of septicaemia, polyarthritis or polyserositis associated with Streptococcus suis infection.CattleTreatment of acute interdigital necrobacillosis in cattle also known as Panaritium or foot rot.Treatment of acute post-partum (puerperal) metritis in cattle, in cases where treatment with another antimicrobial has failed.
适用物种Pigs; Cattle
兽用药物ATC编码QJ01DD90
首次发布日期2017/03/23
修订日期2020/08/25
产品信息https://www.ema.europa.eu/en/documents/product-information/naxcel-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/veterinary/EPAR/naxcel
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