欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号PT/H/0187/001
药品名称Sumatriptano Generis 50 mg Comprimidos
活性成分
    • sumatriptan 50.0 mg
剂型Film-coated tablet
上市许可持有人Old RMS: SE, proc.no: SE/H/0617/01/MR Generis Farmacêutica, S.A. Office Park da Beloura - Edifício 4 - Quinta da Beloura Sintra
参考成员国 - 产品名称Portugal (PT)
互认成员国 - 产品名称
    许可日期2008/04/05
    最近更新日期2014/09/09
    药物ATC编码
      • N02CC01 sumatriptan
    申请类型
    • TypeLevel1:Abridged
    • TypeLevel2:Initial Application
    • TypeLevel3:Generic Art 10.1 and 10.2 Dir 2001/83/EC
    • TypeLevel4:Chemical Substance
    • TypeLevel5:Prescription Only
    附件文件下载
      市场状态Withdrawn(注:已撤市)
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