欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号IT/H/0375/003
药品名称Prestalia 14 mg + 10 mg tablets
活性成分
    • amlodipine 10.0 mg
    • PERINDOPRIL ARGININE 14.0 mg
剂型Tablet
上市许可持有人Les Laboratoires Servier 50, rue Carnot 922284 Suresnes Cedex France
参考成员国 - 产品名称Italy (IT)
互认成员国 - 产品名称
    • Netherlands (NL)
    • Austria (AT)
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Greece (GR)
      PRESTALIA
    • Finland (FI)
    • Latvia (LV)
    • Estonia (EE)
    • Hungary (HU)
    • Czechia (CZ)
      PRESTALIA 14 mg/10 mg, tablety
许可日期2015/03/20
最近更新日期2015/06/30
药物ATC编码
    • C09BB04 perindopril and amlodipine
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Full Dossier Art 8.3(i) Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
附件文件下载
    市场状态Withdrawn(注:已撤市)
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