欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Orlaam
适用类别Human
治疗领域Opioid-Related Disorders
通用名/非专利名称levacetylmethadol
活性成分levacetylmethadol
产品号EMEA/H/C/000077
患者安全信息No
许可状态Withdrawn
ATC编码N02AC
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1997/07/01
上市许可开发者/申请人/持有人Sipaco Internacional Lda.
人用药物治疗学分组Analgesics
兽用药物治疗学分组
欧盟委员会决定日期2002/06/11
修订号
治疗适应症ORLAAM is indicated for the substitution maintenance treatment of opiate addiction in adults previously treated with methadone, as part of a comprehensive treatment plan including medical, social and psychological care. ORLAAM should be administered under the supervision of physicians with experience in addiction treatment and whenever practicable, in centres specialising in the treatment of drug addiction. ORLAAM is not intended for take home use.
适用物种
兽用药物ATC编码
首次发布日期2002/06/11
最后更新日期2002/06/30
产品说明书
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/orlaam
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