欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/3405/002
药品名称Amlodipine/Valsartan Sandoz 5 mg/160 mg, filmomhulde tabletten
活性成分
    • amlodipine besilate 5.0 mg
    • valsartan 160.0 mg
剂型Film-coated tablet
上市许可持有人Sandoz B.V. Veluwezoom 22 1327 AH Almere The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Amlodipine/Valsartan Sandoz 5 mg/160 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Germany (DE)
      Amlodipin/Valsratan 1 A Pharma 5 mg/160 mg
    • Belgium (BE)
      Amlodipine/Valsartan Sandoz 5 mg/160 mg filmomhulde tabletten
    • Austria (AT)
      Amlodipin/Valsartan Sandoz 5 mg/160 mg - Filmtabletten
    • France (FR)
    • Spain (ES)
    • Greece (GR)
      AMLODIPINE+VALSARTAN/SANDOZ
    • Hungary (HU)
    • Slovakia (SK)
      Amlodipín/Valsartan Sandoz 5 mg/160 mg
许可日期2016/04/15
最近更新日期2024/01/22
药物ATC编码
    • C09DB01 valsartan and amlodipine
申请类型
  • TypeLevel1:Known Active Substance
  • 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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