欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号IE/H/1150/002
药品名称AMLODIPINE/VALSARTAN Krka 5 mg/160 mg film-coated tablet
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Krka, d.d., Novo mesto (SI) EL: TAD Pharma GmbH (DE)
参考成员国 - 产品名称Ireland (IE)
互认成员国 - 产品名称
    • Hungary (HU)
      AMLODIPIN/VALZARTÁN KRKA 5 mg/160 mg filmtabletta
    • Belgium (BE)
      Amlodipine/Valsartan Krka 5 mg/160 mg filmohulde tabletten
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Greece (GR)
      AMLODIPINE+VALSARTAN/TAD
    • Norway (NO)
      Amlodipin/Valsartan Krka
    • Finland (FI)
    • Austria (AT)
    • Sweden (SE)
许可日期2015/12/18
最近更新日期2023/08/01
药物ATC编码
    • C09DB01 valsartan and amlodipine
申请类型
  • TypeLevel1:[not specified]
  • TypeLevel2:[not specified]
  • TypeLevel3:[not specified]
  • TypeLevel4:[not specified]
  • TypeLevel5:[not specified]
附件文件下载
市场状态Positive
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