欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/2910/001
药品名称Converide 150 mg/12,5 mg filmomhulde tabletten
活性成分
    • hydrochlorothiazide 12.5 mg
    • irbesartan 150.0 mg
剂型Film-coated tablet
上市许可持有人Medochemie Ltd. 1-10 Constantinoupoleos street 3011 Limassol Cyprus
参考成员国 - 产品名称Netherlands (NL)
Converide 150 mg/12,5 mg filmomhulde tabletten
互认成员国 - 产品名称
    • Greece (GR)
      CONVERIUM PLUS
    • Lithuania (LT)
      CONVERIDE 150 mg/12,5 mg plėvele dengtos tabletės
    • Cyprus (CY)
      Converium Plus 150 mg/12.5 mg FC TABS
    • Czechia (CZ)
      CONVERIDE 150 MG/12,5 MG
    • Romania (RO)
      Converide 150 mg/12,5 mg comprimate filmate
    • Spain (ES)
    • Bulgaria (BG)
      CONVERIDE
    • Malta (MT)
    • Portugal (PT)
许可日期2014/04/28
最近更新日期2024/04/13
药物ATC编码
    • C09DA04 irbesartan 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
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市场状态Positive
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