欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Budesonide/Formoterol Teva Pharma B.V.
适用类别Human
治疗领域Asthma
通用名/非专利名称budesonide;formoterol fumarate dihydrate
活性成分Budesonide;formoterol
产品号EMEA/H/C/003953
患者安全信息No
许可状态Withdrawn
ATC编码R03AK07
是否额外监管No
是否仿制药或hybrid药物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
上市许可日期2014/11/19
上市许可开发者/申请人/持有人Teva Pharma B.V.
人用药物治疗学分组Drugs for obstructive airway diseases
兽用药物治疗学分组
欧盟委员会决定日期2016/12/16
修订号1
治疗适应症Budesonide/Formoterol Teva Pharma B.V. is indicated in adults 18 years of age and older only. AsthmaBudesonide/Formoterol Teva Pharma B.V. is indicated in the regular treatment of asthma, where use of a combination (inhaled corticosteroid and long-acting ?2 adrenoceptor agonist) is appropriate:   or in patients not adequately controlled with inhaled corticosteroids and “as needed” inhaled short-acting ?2 adrenoceptor agonists. in patients already adequately controlled on both inhaled corticosteroids and long-acting ?2 adrenoceptor agonists.  
适用物种
兽用药物ATC编码
首次发布日期2016/12/16
最后更新日期2017/01/30
产品说明书https://www.ema.europa.eu/en/documents/product-information/budesonide/formoterol-teva-pharma-bv-epar-product-information-withdrawn_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/budesonide-formoterol-teva-pharma-bv
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