欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Adrovance
适用类别Human
治疗领域Osteoporosis, Postmenopausal
通用名/非专利名称alendronic acid, colecalciferol
活性成分colecalciferol, alendronic acid (as sodium trihydrate)
产品号EMEA/H/C/000759
患者安全信息no
授权状态Authorised
ATC编码M05BB03
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2007/01/04
上市许可持有人/公司名称N.V. Organon
人用药物治疗分组Drugs for treatment of bone diseases
审评意见发布日期2006/10/18
决定日期2023/10/04
修订号25
适应症Treatment of postmenopausal osteoporosis in patients at risk of vitamin-D insufficiency.Adrovance reduces the risk of vertebral and hip fractures.
首次发布日期2018/07/06
修订日期2023/10/04
产品信息https://www.ema.europa.eu/en/documents/product-information/adrovance-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/adrovance
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