欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Ranibizumab Midas
适用类别Human
治疗领域Wet Macular Degeneration;Macular Edema;Choroidal Neovascularization;Diabetes Complications
通用名/非专利名称ranibizumab
活性成分ranibizumab
产品号EMEA/H/C/006528
患者安全信息No
许可状态Authorised
ATC编码S01LA04
是否额外监管No
是否仿制药或hybrid药物No
是否生物类似药Yes
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2024/09/19
上市许可开发者/申请人/持有人Midas Pharma GmbH
人用药物治疗学分组Ophthalmologicals
兽用药物治疗学分组
审评意见日期2024/07/25
修订号
治疗适应症Treatment of neovascular (wet) age-related macular degeneration (AMD), visual impairment due to diabetic macular oedema (DME), proliferative diabetic retinopathy (PDR), visual impairment due to macular oedema secondary to retinal vein occlusion (branch RVO or central RVO) and visual impairment due to choroidal neovascularisation (CNV).
适用物种
兽用药物ATC编码
首次发布日期2024/07/26
最后更新日期2024/10/29
产品说明书https://www.ema.europa.eu/en/documents/product-information/ranibizumab-midas-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/ranibizumab-midas
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