欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号PT/H/1962/003
药品名称Amlodipina + Olmesartan medoxomilo Generis
活性成分
    • amlodipine 10.0 mg
    • olmesartan medoxomil 40.0 mg
剂型Film-coated tablet
上市许可持有人Generis Farmacêutica, S.A.
参考成员国 - 产品名称Portugal (PT)
互认成员国 - 产品名称
    • Romania (RO)
      Amlodipina/Olmesartan Aurobindo 10 mg/40 mg comprimate filmate
    • Germany (DE)
      Olmesartan/Amlodipin PUREN 40 mg/10 mg Filmtabletten
    • Belgium (BE)
      Olmesartan/Amlodipine AB 40 mg/10 mg filmomhulde tabletten
    • Netherlands (NL)
    • Spain (ES)
许可日期2021/04/08
最近更新日期2024/07/05
药物ATC编码
    • C09DB02 olmesartan medoxomil and amlodipine
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Positive
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