欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/3522/001
药品名称Perindopril Tosilaat/Indapamide Teva 10 mg/2,5 mg, filmomhulde tabletten
活性成分
    • indapamide 2.5 mg
    • perindopril tosilate 10.0 mg
剂型Film-coated tablet
上市许可持有人Teva Nederland B.V. Swensweg 5 2031 GA Haarlem The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Perindopril Tosilaat/Indapamide Teva 10 mg/2,5 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Belgium (BE)
      Coperindo 10 mg/2,5 mg filmomhulde tabletten
    • Ireland (IE)
    • France (FR)
    • Portugal (PT)
    • Italy (IT)
    • Poland (PL)
      Indix Combi
    • Latvia (LV)
      Perindopril/Indapamide Teva 10 mg/2,5 mg apvalkotās tabletes
    • Lithuania (LT)
      Perindopril/Indapamide Teva 10 mg/2,5 mg plėvele dengtos tabletės
    • Estonia (EE)
      PERINDOPRIL/INDAPAMIDE TEVA
    • Romania (RO)
      Perindopril Tosilat/Indapamidă Teva 10 mg/2,5 mg comprimate filmate
    • Croatia (HR)
      Co-Articel 10 mg/2,5 mg filmom obložene tablete
许可日期2016/10/12
最近更新日期2024/05/23
药物ATC编码
    • C09BA04 perindopril and diuretics
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
附件文件下载
市场状态Positive
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