欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Cymbalta
适用类别Human
治疗领域Anxiety Disorders; Diabetic Neuropathies; Depressive Disorder, Major
通用名/非专利名称duloxetine
活性成分duloxetine
产品号EMEA/H/C/000572
患者安全信息no
授权状态Authorised
ATC编码N06AX21
是否额外监管no
是否仿制药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
批准上市日期2004/12/17
上市许可持有人/公司名称Eli Lilly Nederland B.V.
人用药物治疗分组Psychoanaleptics,
审评意见发布日期2004/09/16
决定日期2021/12/14
修订号32
适应症Treatment of major depressive disorder.Treatment of diabetic peripheral neuropathic pain.Treatment of generalised anxiety disorder.Cymbalta is indicated in adults.
首次发布日期2017/01/26
修订日期2023/06/27
产品信息https://www.ema.europa.eu/en/documents/product-information/cymbalta-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/cymbalta
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