欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号HU/H/0644/003
药品名称Lisinopril/Amlodipine Alkaloid-INT 20 mg/5 mg tablet
活性成分
    • Amlodipine besilate 20.0 mg
    • Lisinopril dihydrate 5.0 mg
剂型Tablet
上市许可持有人Alkaloid-INT d.o.o. Šlandrova ulica 4 Ljubljana-Črnuče 1231 Slovenia Telephone + 386 1 300 42 90 E-mail info@alkaloid.si
参考成员国 - 产品名称Hungary (HU)
LISINOPRIL/AMLODIPINE ALKALOID-INT 20 mg/5 mg tabletta
互认成员国 - 产品名称
    • Portugal (PT)
    • Poland (PL)
    • Bulgaria (BG)
      Lisinopril/Amlodipine Alkaloid-INT
    • Slovenia (SI)
    • Malta (MT)
    • Croatia (HR)
      Skopryl Combo 20 mg/5 mg tablete
许可日期2020/08/26
最近更新日期2025/05/15
药物ATC编码
    • C09BB03 lisinopril and amlodipine
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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