欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Emtricitabine / Tenofovir alafenamide Viatris
适用类别Human
治疗领域HIV Infections
通用名/非专利名称emtricitabine;tenofovir alafenamide
活性成分emtricitabine;tenofovir alafenamide fumarate
产品号EMEA/H/C/006469
患者安全信息No
许可状态Authorised
ATC编码J05AR17
是否额外监管No
是否仿制药或hybrid药物Yes
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2025/07/18
上市许可开发者/申请人/持有人Viatris Limited
人用药物治疗学分组Antivirals for systemic use
兽用药物治疗学分组
审评意见日期2025/05/22
欧盟委员会决定日期2025/07/18
修订号
治疗适应症Emtricitabine/Tenofovir alafenamide Viatris is indicated in combination with other antiretroviral agents for the treatment of adults and adolescents (aged 12 years and older with body weight at least 35 kg) infected with human immunodeficiency virus type 1 (HIV-1).
适用物种
兽用药物ATC编码
首次发布日期2025/05/23
最后更新日期2025/08/05
产品说明书https://www.ema.europa.eu/en/documents/product-information/emtricitabine-tenofovir-alafenamide-viatris-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/emtricitabine-tenofovir-alafenamide-viatris
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