欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号HU/H/0248/002
药品名称Amlator-P
活性成分
    • amlodipine besilate 10.0 mg
    • atorvastatin lysin salt 10.0 mg
剂型Film-coated tablet
上市许可持有人Gedeon Richter Plc. Gyömrői út 19-21. H-1103 Budapest Hungary
参考成员国 - 产品名称Hungary (HU)
AMLATOR 10 mg/10 mg filmtabletta
互认成员国 - 产品名称
    • Poland (PL)
      Amlator
    • Bulgaria (BG)
      Amlator
    • Czechia (CZ)
      Amlator-P 10 mg/10 mg potahované tablety
    • Romania (RO)
      Duplecor 10 mg/10 mg comprimate filmate
    • Slovakia (SK)
      Amlator 10 mg/10 mg filmom obalené tablety
许可日期2011/03/09
最近更新日期2024/03/19
药物ATC编码
    • C10BX03 atorvastatin and amlodipine
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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