欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Zoledronic acid Mylan
适用类别Human
治疗领域Fractures, Bone
通用名/非专利名称zoledronic acid
活性成分zoledronic acid
产品号EMEA/H/C/002482
患者安全信息No
许可状态Authorised
ATC编码M05BA08
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2012/08/23
上市许可开发者/申请人/持有人Mylan Pharmaceuticals Limited
人用药物治疗学分组Drugs for treatment of bone diseases
兽用药物治疗学分组
欧盟委员会决定日期2025/11/06
修订号17
治疗适应症Prevention of skeletal related events (pathological fractures, spinal compression, radiation or surgery to bone, or tumour-induced hypercalcaemia) in adult patients with advanced malignancies involving bone; treatment of adult patients with tumour-induced hypercalcaemia (TIH).
适用物种
兽用药物ATC编码
首次发布日期2017/09/11
最后更新日期2025/11/07
产品说明书https://www.ema.europa.eu/en/documents/product-information/zoledronic-acid-mylan-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/zoledronic-acid-mylan
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