欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号IE/H/1240/001
药品名称Perindopril arginin/Amlodipine besilate/Indapamide 5mg/5mg/1.25mg
活性成分
    • AMLODIPINE BESILATE 5.0 mg
    • indapamide 1.25 mg
    • PERINDOPRIL ARGININE 5.0 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Ireland (IE)
互认成员国 - 产品名称
    • Hungary (HU)
      CO-DALNESSA-AS 5 mg/1,25 mg/5 mg, 10/2,5/5 mg, 10/2,5/10 mg tabletta
    • Bulgaria (BG)
      Co-Amlessa Neo
    • Cyprus (CY)
      CO-APERNEVA 5 mg/1,25 mg/5 mg δισκία
    • Czechia (CZ)
      Tonanda Neo
    • Germany (DE)
      Co-Amlessa 5 mg/1,25 mg/5 mg Tabletten
    • Romania (RO)
      Co-Amlessaneo 5 mg/1,25 mg/5 mg comprimate
    • Belgium (BE)
    • Slovakia (SK)
    • Portugal (PT)
    • Slovenia (SI)
    • Greece (GR)
    • Croatia (HR)
    • Poland (PL)
    • Latvia (LV)
    • Lithuania (LT)
      Perindopril arginine/indapamide/amlodipine Krka 5 mg/1,25 mg/5 mg tabletės
    • Estonia (EE)
许可日期2024/03/14
最近更新日期2024/03/14
药物ATC编码
    • C09BX01 perindopril, amlodipine and indapamide
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Generic Art 10.1 and 10.2 Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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