欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号AT/H/0705/002
药品名称Olmesartan/Amlodipin Sandoz 40 mg/5 mg – Filmtabletten
活性成分
    • amlodipine 5.0 mg
    • olmesartan medoxomil 40.0 mg
剂型Film-coated tablet
上市许可持有人Sandoz GmbH Biochemiestrasse 10 6250 Kundl, Austria
参考成员国 - 产品名称Austria (AT)
Olmesartan/Amlodipin Sandoz 40 mg/5 mg – Filmtabletten
互认成员国 - 产品名称
    • Belgium (BE)
      Olmesartan/Amlodipine Sandoz 40 mg/5 mg filmomhulde tabletten
    • Spain (ES)
    • Greece (GR)
      OLMESARTAN+AMLODIPINE/SANDOZ
    • Lithuania (LT)
      Olmesartan medoxomil/Amlodipine Sandoz 40 mg / 5 mg plėvele dengtos tabletės
    • Germany (DE)
      OlmeAmlo-1 A Pharma 40 mg/5 mg Filmtabletten
许可日期2017/09/13
最近更新日期2024/01/11
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
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市场状态Positive
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