欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号HU/H/0484/002
药品名称Roxiper 4 mg/1.25 mg/20 mg filmtabletta
活性成分
    • indapamide 1.25 mg
    • perindopril 4.0 mg
    • rosuvastatin 20.0 mg
剂型Film-coated tablet
上市许可持有人KRKA, d.d., Novo mesto Šmarješka cesta 6 Novo mesto 8501 Slovenia Telephone +38673319037 Telefax +38673322742
参考成员国 - 产品名称Hungary (HU)
ROXIPER 20 mg/4 mg/1,25 mg filmtabletta
互认成员国 - 产品名称
    • Portugal (PT)
    • Finland (FI)
    • Poland (PL)
    • Latvia (LV)
      Triemma 20 mg/4 mg/1,25 mg apvalkotās tabletes
    • Lithuania (LT)
      Roxiper 20 mg/4 mg/1,25 mg plėvele dengtos tabletės
    • Estonia (EE)
      ROXIPER
    • Bulgaria (BG)
      Roxiper
    • Romania (RO)
    • Slovakia (SK)
      Roxiper 20 mg/4 mg/1,25 mg filmom obalené tablety
    • Slovenia (SI)
      Roxiper 20 mg/4 mg/1,25 mg filmsko obložene tablete
许可日期2018/07/25
最近更新日期2024/08/22
药物ATC编码
    • C10BX Lipid modifying agents in combination with other drugs
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
附件文件下载
市场状态Positive
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