欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号EE/H/0400/001
药品名称Nesyrgy
活性成分
    • Amlodipine besilate 5.0 mg
    • Nebivolol hydrochloride 5.0 mg
剂型Film-coated tablet
上市许可持有人Menarini International Operations Luxembourg S.A. 1 Avenue De La Gare Luxembourg 1611 Luxembourg
参考成员国 - 产品名称Estonia (EE)
互认成员国 - 产品名称
    • Bulgaria (BG)
      Nesyrgy 5mg/5mg film-coated tablets
    • Ireland (IE)
    • Cyprus (CY)
      Nesyrgy film-coated tablet, 5 mg/5 mg
    • Austria (AT)
    • Czechia (CZ)
      Nesyrgy
    • France (FR)
    • Romania (RO)
      NESYRGY 5 mg/5 mg comprimate filmate
    • Spain (ES)
    • Slovakia (SK)
    • Portugal (PT)
    • Slovenia (SI)
    • Italy (IT)
    • Croatia (HR)
    • Greece (GR)
    • Poland (PL)
    • Latvia (LV)
    • Lithuania (LT)
      Kliqqo 5 mg/5 mg plėvele dengtos tabletės
    • Belgium (BE)
    • Hungary (HU)
      Nesyrgy 5 mg/ 5 mg filmtabletta
    • Luxembourg (LU)
许可日期2024/10/16
最近更新日期2024/10/17
药物ATC编码
    • C07FB12 nebivolol 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
附件文件下载
市场状态Positive
©2006-2025 Drugfuture->European Union HMA Authorisation of Medicines DataBase