欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/2636/001
药品名称TRIPLIXAM 2,5 mg/0,625 mg/5 mg, filmomhulde tabletten
活性成分
    • amlodipine 5.0 mg
    • indapamide 625.0 µg
    • perindopril arginine salt 2.5 mg
剂型Film-coated tablet
上市许可持有人Les Laboratoires Servier 50 rue Carnot 92284 Suresnes Cedex France
参考成员国 - 产品名称Netherlands (NL)
Triplixam 2,5 mg/0,625mg/5 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Belgium (BE)
    • Luxembourg (LU)
    • Ireland (IE)
    • Austria (AT)
    • France (FR)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Finland (FI)
    • Poland (PL)
    • Latvia (LV)
    • Lithuania (LT)
    • Hungary (HU)
    • Bulgaria (BG)
    • Cyprus (CY)
    • Romania (RO)
    • Slovakia (SK)
    • Slovenia (SI)
    • Malta (MT)
    • Croatia (HR)
许可日期2013/12/17
最近更新日期2022/11/24
药物ATC编码
    • C09BX01 perindopril, amlodipine and indapamide
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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