欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/1896/002
药品名称Remifentanil 2 mg
活性成分
    • remifentanil hydrochloride 2.0 mg
剂型Powder for solution for infusion/injection
上市许可持有人Sandoz B.V. Veluwezoom 22 1327 AH Almere The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Remifentanil Sandoz 2 mg, poeder voor oplossing voor injectie of infusie
互认成员国 - 产品名称
    许可日期2010/12/09
    最近更新日期2018/12/19
    药物ATC编码
      • N01AH06 remifentanil
    申请类型
    • TypeLevel1:Abridged
    • TypeLevel2:Additional Strength/Form
    • 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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