欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号CZ/H/0677/004
药品名称Telassmo 80 mg/ 10 mg tablet
活性成分
    • amlodipine 10.0 mg
    • telmisartan 80.0 mg
剂型Tablet
上市许可持有人Krka, d.d., Novo mesto Šmarješka cesta 6 8501 Novo mesto Slovenia
参考成员国 - 产品名称Czechia (CZ)
TELASSMO
互认成员国 - 产品名称
    • Portugal (PT)
    • Latvia (LV)
      Telassmo 80 mg/10 mg tabletes
    • Estonia (EE)
      TELDIPIN
    • Bulgaria (BG)
      Teldipin
    • Romania (RO)
      TELASSMO 80 mg/10 mg comprimate
    • Slovakia (SK)
      Teldipin 80 mg/10 mg tablety
    • Slovenia (SI)
许可日期2016/11/15
最近更新日期2024/08/30
药物ATC编码
    • C09DB04 telmisartan and amlodipine
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Additional Strength/Form
  • TypeLevel3:Fixed combination Art 10b 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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