欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DK/H/2095/001
药品名称Zoledronsyre "Sigillata"
活性成分
    • zoledronic acid 0.8 mg/ml
剂型Concentrate for solution for infusion
上市许可持有人Sigillata Limited NW19 7JH London United Kingdom
参考成员国 - 产品名称Denmark (DK)
Zoledronsyre "Sigillata"
互认成员国 - 产品名称
    许可日期2012/03/15
    最近更新日期2017/04/18
    药物ATC编码
      • M05BA08 zoledronic acid
    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)
    ©2006-2025 Drugfuture->European Union HMA Authorisation of Medicines DataBase