欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Arepanrix
适用类别Human
治疗领域Influenza, Human;Immunization;Disease Outbreaks
通用名/非专利名称pandemic influenza vaccine (H1N1)v (split virion, inactivated, adjuvanted)
活性成分split influenza virus, inactivated, containing antigen*: A/California/7/2009 (H1N1)v like strain (X-179A)*propagated in eggs.
产品号EMEA/H/C/001201
患者安全信息No
许可状态Withdrawn
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Yes
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2010/03/23
上市许可开发者/申请人/持有人GlaxoSmithKline Biologicals S.A.
人用药物治疗学分组Influenza vaccines
兽用药物治疗学分组
欧盟委员会决定日期2010/08/13
修订号1
治疗适应症Prophylaxis of influenza in an officially declared pandemic situation. Pandemic influenza vaccine should be used in accordance with official guidance
适用物种
兽用药物ATC编码
首次发布日期2010/08/13
最后更新日期2011/10/25
产品说明书https://www.ema.europa.eu/en/documents/product-information/arepanrix-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/arepanrix
©2006-2025 DrugFuture->European Medicines Agency Authorisation of Medicines DataBase