欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Aldara
适用类别Human
治疗领域Condylomata Acuminata;Keratosis;Keratosis, Actinic;Carcinoma, Basal Cell
通用名/非专利名称imiquimod
活性成分imiquimod
产品号EMEA/H/C/000179
患者安全信息No
许可状态Authorised
ATC编码D06BB10
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1998/09/18
上市许可开发者/申请人/持有人Viatris Healthcare Limited
人用药物治疗学分组Antibiotics and chemotherapeutics for dermatological use
兽用药物治疗学分组
审评意见日期1998/05/27
欧盟委员会决定日期2025/07/17
修订号33
治疗适应症Imiquimod cream is indicated for the topical treatment of : External genital and perianal warts (condylomata acuminata) in adults. Small superficial basal cell carcinomas (sBCCs) in adults. Clinically typical, nonhyperkeratotic, nonhypertrophic actinic keratoses (AKs) on the face or scalp in immunocompetent adult patients when size or number of lesions limit the efficacy and/or acceptability of cryotherapy and other topical treatment options are contraindicated or less appropriate.
适用物种
兽用药物ATC编码
首次发布日期2018/06/29
最后更新日期2025/07/18
产品说明书https://www.ema.europa.eu/en/documents/product-information/aldara-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/aldara
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