欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Supemtek
适用类别Human
治疗领域Influenza, Human
通用名/非专利名称trivalent influenza vaccine (recombinant, prepared in cell culture)
活性成分A/California/07/2009 (H1N1)pdm09-like strain (A/California/07/2009);A/Texas/50/2012 (H3N2)-like strain (A/Texas/50/2012);B/Brisbane/60/2008-like strain (B/Brisbane/60/2008)
产品号EMEA/H/C/006674
患者安全信息No
许可状态Authorised
ATC编码J07BB02
是否额外监管No
是否仿制药或hybrid药物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
上市许可日期2026/03/30
上市许可开发者/申请人/持有人Sanofi Winthrop Industrie
人用药物治疗学分组Vaccines
兽用药物治疗学分组
审评意见日期2026/01/29
修订号
治疗适应症Supemtek is indicated for active immunisation for the prevention of influenza disease in adults and children from 9 years of age and older. Supemtek should be used in accordance with official recommendations.
适用物种
兽用药物ATC编码
首次发布日期2026/01/30
最后更新日期2026/04/08
产品说明书https://www.ema.europa.eu/en/documents/product-information/supemtek-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/supemtek
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