欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号PT/H/1429/001
药品名称Olmesartan medoxomil Sandoz Farmacêutica
活性成分
    • Olmesartan medoxomil 10.0 mg
剂型Film-coated tablet
上市许可持有人Sandoz Farmacêutica, Lda.
参考成员国 - 产品名称Portugal (PT)
互认成员国 - 产品名称
    • Germany (DE)
      Olmesartan – 1 A Pharma 10 mg Filmtabletten
    • Belgium (BE)
      Olmesartan Sandoz 10 mg filmomhulde tabletten
    • Netherlands (NL)
    • Ireland (IE)
    • Italy (IT)
    • Greece (GR)
    • Bulgaria (BG)
      olmesartan Sandoz
许可日期2016/02/24
最近更新日期2025/02/07
药物ATC编码
    • C09CA08 olmesartan medoxomil
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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