欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Ribavirin Teva Pharma B.V.
适用类别Human
治疗领域Hepatitis C, Chronic
通用名/非专利名称ribavirin
活性成分ribavirin
产品号EMEA/H/C/001064
患者安全信息No
许可状态Withdrawn
ATC编码J05AP01
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2009/07/01
上市许可开发者/申请人/持有人Teva B.V.
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2009/04/23
欧盟委员会决定日期2021/06/22
修订号14
治疗适应症Ribavirin Teva Pharma B.V. is indicated in combination with other medicinal products for the treatment of chronic hepatitis C (CHC) in adults (see sections 4.2, 4.4, and 5.1). Ribavirin Teva Pharma B.V. is indicated in combination with other medicinal products for the treatment of chronic hepatitis C (CHC) for paediatric patients (children 3 years of age and older and adolescents) not previously treated and without liver decompensation (see sections 4.2, 4.4 and 5.1).
适用物种
兽用药物ATC编码
首次发布日期2016/11/04
最后更新日期2021/07/09
产品说明书https://www.ema.europa.eu/en/documents/product-information/ribavirin-teva-pharma-bv-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/ribavirin-teva-pharma-bv
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