欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Pregabalin Sandoz
适用类别Human
治疗领域Anxiety Disorders;Neuralgia;Epilepsy
通用名/非专利名称pregabalin
活性成分pregabalin
产品号EMEA/H/C/004010
患者安全信息No
许可状态Authorised
ATC编码N02BF02
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2015/06/19
上市许可开发者/申请人/持有人Sandoz GmbH
人用药物治疗学分组Other analgesics and antipyretics
兽用药物治疗学分组
审评意见日期2015/04/23
欧盟委员会决定日期2025/12/02
修订号23
治疗适应症Neuropathic pain Pregabalin Sandoz is indicated for the treatment of peripheral and central neuropathic pain in adults. Epilepsy Pregabalin Sandoz is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation. Generalised Anxiety Disorder Pregabalin Sandoz is indicated for the treatment of Generalised Anxiety Disorder (GAD) in adults.
适用物种
兽用药物ATC编码
首次发布日期2018/02/05
最后更新日期2025/12/02
产品说明书https://www.ema.europa.eu/en/documents/product-information/pregabalin-sandoz-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/pregabalin-sandoz
©2006-2025 DrugFuture->European Medicines Agency Authorisation of Medicines DataBase