欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号PL/H/0940/002
药品名称Carditrat 8 mg + 10 mg capsules, hard
活性成分
    • Amlodipine 10.0 mg
    • candesartancilexetil 8.0 mg
剂型Capsule, hard
上市许可持有人Uni-Pharma Kleon Tsetis Pharmaceutical Laboratories S.A 14th km National Road 1 145 64 Kifisia, Greece
参考成员国 - 产品名称Poland (PL)
Carditrat
互认成员国 - 产品名称
    • Greece (GR)
    • Cyprus (CY)
      Carditrat 8 mg + 10 mg capsules, hard
许可日期2025/02/12
最近更新日期2025/02/12
药物ATC编码
    • C09DB07 candesartan and amlodipine
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Full Dossier Art 8.3(i) 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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