欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Busulfan Fresenius Kabi
适用类别Human
治疗领域Hematopoietic Stem Cell Transplantation
通用名/非专利名称busulfan
活性成分busulfan
产品号EMEA/H/C/002806
患者安全信息No
许可状态Authorised
ATC编码L01AB01
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2014/09/22
上市许可开发者/申请人/持有人Fresenius Kabi Deutschland GmbH
人用药物治疗学分组Alkyl sulfonates
兽用药物治疗学分组
审评意见日期2014/07/25
欧盟委员会决定日期2025/07/01
修订号11
治疗适应症Busulfan Fresenius Kabi followed by cyclophosphamide (BuCy2) is indicated as conditioning treatment prior to conventional haematopoietic progenitor cell transplantation (HPCT) in adult patients when the combination is considered the best available option. Busulfan Fresenius Kabi followed by cyclophosphamide (BuCy4) or melphalan (BuMel) is indicated as conditioning treatment prior to conventional haematopoietic progenitor cell transplantation in paediatric patients.
适用物种
兽用药物ATC编码
首次发布日期2018/05/08
最后更新日期2025/07/01
产品说明书https://www.ema.europa.eu/en/documents/product-information/busulfan-fresenius-kabi-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/busulfan-fresenius-kabi
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