欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/6348/002
药品名称Olmesartan/Amlodipin/HCT-ratiopharm 40 mg/ 5 mg/ 12,5 mg Filmtabletten
活性成分
    • Amlodipine 5.0 mg
    • Hydrochlorothiazide 12.5 mg
    • Olmesartan medoxomil 40.0 mg
剂型Film-coated tablet
上市许可持有人ratiopharm GmbH Graf-Arco-Str. 3 89079 Ulm Germany
参考成员国 - 产品名称Germany (DE)
Olmesartan/Amlodipin/HCT-ratiopharm 40 mg/ 5 mg/ 12,5 mg Filmtabletten
互认成员国 - 产品名称
    • Netherlands (NL)
    • Spain (ES)
    • Latvia (LV)
      Olmesartan medoxomil/Amlodipine/Hydrochlorthiazide Teva 40 mg/5 mg/12,5 mg apvalkotās tabletes
    • Lithuania (LT)
      Olmesartan medoxomil/Amlodipine/Hydrochlorothiazide Teva 40 mg/5 mg/12,5 mg plėvele dengtos tabletės
    • Bulgaria (BG)
      Olmesta A Plus
许可日期2020/11/12
最近更新日期2024/09/19
药物ATC编码
    • C09DX03 olmesartan medoxomil, amlodipine and hydrochlorothiazide
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
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市场状态Positive
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