欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/3724/003
药品名称Olmesartan medoxomil/Amlodipine TEVA 40mg/10mg
活性成分
    • AMLODIPINE BESILATE 10.0 mg
    • olmesartan medoxomil 40.0 mg
剂型Film-coated tablet
上市许可持有人TEVA Nederland B.V. Swensweg 5 2031 GA Nederland
参考成员国 - 产品名称Netherlands (NL)
Olmesartan medoxomil/Amlodipine TEVA 40mg/10mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Germany (DE)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Latvia (LV)
      Olmesartan medoxomil/Amlodipine Teva 40 mg/10 mg apvalkotās tabletes
    • Lithuania (LT)
      Olmesartan medoxomil/Amlodipine Teva 40 mg/10 mg plėvele dengtos tabletės
许可日期2017/09/27
最近更新日期2024/04/23
药物ATC编码
    • C09DB02 olmesartan medoxomil and amlodipine
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Positive
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