欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/6053/003
药品名称Olmesartan/Amlodipine/Hydrochlorothiazide Glenmark 40 mg/10 mg/12.5 mg Filmtabletten
活性成分
    • AMLODIPINE BESILATE 13.87 mg
    • hydrochlorothiazide 12.5 mg
    • olmesartan medoxomil 40.0 mg
剂型Film-coated tablet
上市许可持有人Glenmark Arzneimittel GmbH Industriestr. 31 D-82194 Gröbenzell Germany
参考成员国 - 产品名称Germany (DE)
Olmesartan/Amlodipine/Hydrochlorothiazide Glenmark 40 mg/10 mg/12.5 mg Filmtabletten
互认成员国 - 产品名称
    • Spain (ES)
许可日期2020/12/08
最近更新日期2023/03/13
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
附件文件下载
市场状态Positive
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