欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号HU/H/0350/004
药品名称TENLORIS 100/10 mg
活性成分
    • Amlodipine besilate 10.0 mg
    • Losartan potassium salt 100.0 mg
剂型Film-coated tablet
上市许可持有人Krka, d.d., Novo mesto Address: Šmarješka cesta 6, 8501 Novo mesto Country: Slovenia
参考成员国 - 产品名称Hungary (HU)
TENLORIS 100 mg/10 mg filmtabletta
互认成员国 - 产品名称
    • Poland (PL)
      Alortia
    • Latvia (LV)
      Tenloris 100 mg/10 mg apvalkotās tabletes
    • Lithuania (LT)
      Tenloris 100 mg/10 mg plėvele dengtos tabletės
    • Bulgaria (BG)
      Tenloris
    • Slovakia (SK)
      Tenloris 100 mg/10 mg filmom obalené tablety
许可日期2014/01/06
最近更新日期2024/10/30
药物ATC编码
    • C09DB06 losartan and amlodipine
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Fixed combination Art 10b Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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