欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号CZ/H/0720/002
药品名称Olmesartan/Amlodipin Zentiva 40 mg/5 mg
活性成分
    • amlodipine besilate 5.0 mg
    • olmesartan medoxomil 40.0 mg
剂型Film-coated tablet
上市许可持有人Zentiva k.s. U Kabelovny 130 10237 Praha 10 - Dolní Měcholupy Czech Republic
参考成员国 - 产品名称Czechia (CZ)
OLMESARTAN/AMLODIPIN ZENTIVA
互认成员国 - 产品名称
    • Germany (DE)
      Olmesartan Amlodipin Zentiva 40 mg/5 mg Filmtabletten
    • United Kingdom (Northern Ireland) (XI)
    • Portugal (PT)
    • Italy (IT)
    • Latvia (LV)
      Olmesartan medoxomil/Amlodipine Zentiva 40 mg/5 mg apvalkotās tabletes
    • Estonia (EE)
      OLMESARTAN MEDOXOMIL/AMLODIPINE ZENTIVA
许可日期2017/09/21
最近更新日期2024/03/22
药物ATC编码
    • C09DB02 olmesartan medoxomil and amlodipine
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Generic Art 10.1 and 10.2 Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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