欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Intanza
适用类别Human
治疗领域Influenza, Human;Immunization
通用名/非专利名称influenza vaccine (split virion, inactivated)
活性成分influenza virus (inactivated, split) of the following strains:A/California/7/2009 (H1N1)pdm09 - like strain (A/California/7/2009, NYMC X-179A)A/Hong Kong/4801/2014 (H3N2) - like strain (A/Hong Kong/4801/2014, NYMC X-263B)B/Brisbane/60/2008 - like strain (B/Brisbane/60/2008, wild type)
产品号EMEA/H/C/000957
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2009/02/24
上市许可开发者/申请人/持有人Sanofi Pasteur Europe
人用药物治疗学分组Vaccines
兽用药物治疗学分组
欧盟委员会决定日期2017/09/07
修订号18
治疗适应症Prophylaxis of influenza in individuals 60 years of age and over, especially in those who run an increased risk of associated complications.The use of Intanza should be based on official recommendations.
适用物种
兽用药物ATC编码
首次发布日期2017/09/07
最后更新日期2018/09/04
产品说明书https://www.ema.europa.eu/en/documents/product-information/intanza-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/intanza
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