欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/6311/004
药品名称Olmesartan/Amlodipin/HCT Heumann 40 mg/10 mg/12,5 mg Filmtabletten
活性成分
    • AMLODIPINE BESILATE 13.86 mg
    • hydrochlorothiazide 12.5 mg
    • olmesartan medoxomil 40.0 mg
剂型Film-coated tablet
上市许可持有人Heumann Pharma GmbH & Co. Generica KG Südwestpark 50 D-90449 Nürnberg Germany
参考成员国 - 产品名称Germany (DE)
Olmesartan/Amlodipin/HCT Heumann 40 mg/10 mg/12,5 mg Filmtabletten
互认成员国 - 产品名称
    许可日期2021/01/18
    最近更新日期2023/09/01
    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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