欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DK/H/3057/005
药品名称Olmesartan/Amlodipine/HCTZ "Krka"
活性成分
    • amlodipine besilate 10.0 mg
    • hydrochlorothiazide 25.0 mg
    • olmesartan medoxomil 40.0 mg
剂型Film-coated tablet
上市许可持有人KRKA d.d. Novo mesto Smarjeska cesta 6 8501 Novo Mesto Slovenia
参考成员国 - 产品名称Denmark (DK)
Olmesartan/Amlodipine/HCTZ "Krka"
互认成员国 - 产品名称
    • Slovenia (SI)
    • Germany (DE)
      OlmeAmlo HCT 40 mg/10 mg/25 mg Filmtabletten
    • Belgium (BE)
      Olmesartan/Amlodipine/HCTZ Krka 40 mg/10 mg/25 mg filmomhulde tabletten
    • Ireland (IE)
    • Spain (ES)
    • Portugal (PT)
    • Greece (GR)
    • Latvia (LV)
      Olsitri 40 mg/10 mg/25 mg apvalkotās tabletes
    • Lithuania (LT)
      Olsitri 40 mg/10 mg/25 mg plėvele dengtos tabletės
    • Estonia (EE)
      OLSITRI
许可日期2020/04/29
最近更新日期2024/04/24
药物ATC编码
    • C CARDIOVASCULAR SYSTEM
    • C09 AGENTS ACTING ON THE RENIN-ANGIOTENSIN SYSTEM
    • C09D ANGIOTENSIN II RECEPTOR BLOCKERS (ARBs), COMBINATIONS
    • C09DX03 olmesartan medoxomil, amlodipine and hydrochlorothiazide
    • C09DX Angiotensin II receptor blockers (ARBs), other combinations
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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