欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/3868/003
药品名称Olmesartan/Amlodipin STADA
活性成分
    • AMLODIPINE BESILATE 10.0 mg
    • Olmesartan medoxomil 40.0 mg
剂型Film-coated tablet
上市许可持有人STADA Arzneimittel AG Stadastrasse 2-18 Bad Vilbel 61118
参考成员国 - 产品名称Netherlands (NL)
Olmesartan/Amlodipine STADA 40 mg/10 mg filmomhulde tabletten
互认成员国 - 产品名称
    • Germany (DE)
      Olmesartan/Amlodipin STADA 40 mg/10 mg Filmtabletten
    • Belgium (BE)
      Olmesartan/Amlodipine EG 40 mg/10 mg filmomhulde tabletten
    • Luxembourg (LU)
    • Ireland (IE)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
许可日期2017/08/10
最近更新日期2024/11/26
药物ATC编码
    • C09DB02 olmesartan medoxomil and amlodipine
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
©2006-2024 Drugfuture->European Union HMA Authorisation of Medicines DataBase