欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号PT/H/1409/001
药品名称Amlodipina + Valsartan Aurovitas
活性成分
    • amlodipine besilate 5.0 mg
    • valsartan 80.0 mg
剂型Film-coated tablet
上市许可持有人Aurovitas Unipessoal, Lda.
参考成员国 - 产品名称Portugal (PT)
互认成员国 - 产品名称
    • Germany (DE)
      Amlodipin/Valsartan Aurobindo 5 mg/80 mg Filmtabletten
    • Netherlands (NL)
      Amlodipine/Valsartan Aurobindo 5/80 mg, filmomhulde tabletten
    • Romania (RO)
      Amlodipină/Valsartan Aurobindo 5 mg/80 mg comprimate filmate
许可日期2015/12/16
最近更新日期2024/04/11
药物ATC编码
    • C09DB01 valsartan 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
附件文件下载
市场状态Positive
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