欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号SK/H/0199/003
药品名称Perindopril amlodipine 8 mg/5 mg tablets
活性成分
    • amlodipine besilate 6.935 mg
    • perindopril tert-butylamine 8.0 mg
剂型Tablet
上市许可持有人Name: Krka d.d., Novo mesto Šmarješka cesta 6, 8501 Novo mesto Slovenia
参考成员国 - 产品名称Slovakia (SK)
互认成员国 - 产品名称
    • United Kingdom (Northern Ireland) (XI)
      PL 01656/0116 - 0016
    • Netherlands (NL)
    • Portugal (PT)
    • Italy (IT)
    • Poland (PL)
      Amlessa
    • Latvia (LV)
    • Lithuania (LT)
      Dalnessa 8 mg/5 mg tabletės
    • Hungary (HU)
      AMLESSA 8 mg/5 mg tabletta
    • Czechia (CZ)
      Amlessa 8 mg/5 mg tablets
    • Romania (RO)
      Amlessa 8 mg/5 mg comprimate
    • Slovenia (SI)
      Amlessa 8 mg/5 mg tablete
许可日期2011/08/05
最近更新日期2023/08/14
药物ATC编码
    • C09BB04 perindopril and amlodipine
申请类型
  • TypeLevel1:[not specified]
  • TypeLevel2:[not specified]
  • TypeLevel3:[not specified]
  • TypeLevel4:[not specified]
  • TypeLevel5:[not specified]
附件文件下载
    市场状态Positive
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