欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/4813/001
药品名称Olmesartan medoxomil/Amlodipine Accord 20/5 mg Filmtabletten
活性成分
    • AMLODIPINE BESILATE 6.95 mg
    • olmesartan medoxomil 20.0 mg
剂型Film-coated tablet
上市许可持有人Accord Healthcare B.V. Winthontlaan 200 3526 KV UTRECHT Netherlands
参考成员国 - 产品名称Germany (DE)
Olmesartan medoxomil/Amlodipine Accord 20/5 mg Filmtabletten
互认成员国 - 产品名称
    • Netherlands (NL)
      Olmesartan medoxomil/Amlodipine Accord 20 mg/5 mg filmomhulde tabletten
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
    • Spain (ES)
    • Italy (IT)
    • Finland (FI)
    • Latvia (LV)
      Olmesartan medoxomil/Amlodipine Accord 20 mg/5 mg apvalkotās tabletes
    • Lithuania (LT)
      Olmesartan medoxomil/Amlodipine Accord 20 mg/5 mg plėvele dengtos tabletės
    • Estonia (EE)
      Olmesartan medoxomil/amlodipine Accord
    • Romania (RO)
许可日期2017/11/08
最近更新日期2024/02/07
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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