欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/1067/001
药品名称Nebiretic 5mg/12,5 mg, filmomhulde tabletten
活性成分
    • Hydrochlorothiazide 12.5 mg
    • Nebivolol 5.0 mg
剂型Film-coated tablet
上市许可持有人Menarini International Operations Luxembourg S.A. Luxembourg Luxembourg
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    • Hungary (HU)
      NEBILET PLUS 5 mg/12,5 mg filmtabletta
    • Bulgaria (BG)
    • Slovakia (SK)
      Nebilet HCTZ 5 mg/12,5 mg
    • Romania (RO)
      Co-Nebilet 5 mg/12,5 mg comprimate filmate
    • Czechia (CZ)
      Nebilet Plus H 5 mg/12,5 mg
    • Cyprus (CY)
      LOBIVON PLUS 5MG/12.5MG
    • Estonia (EE)
      Nebilet Plus
    • Lithuania (LT)
      Nebilet Plus 5 mg/12,5 mg plėvele dengtos tabletės
    • Latvia (LV)
      Nebilet Plus 5 mg/12,5 mg apvalkotās tabletes
    • Poland (PL)
      Nebilet HCT
    • Finland (FI)
    • Greece (GR)
    • Italy (IT)
    • Portugal (PT)
    • Spain (ES)
    • France (FR)
    • Ireland (IE)
    • Belgium (BE)
    • Denmark (DK)
      hypoloc comp
    • Luxembourg (LU)
    • Malta (MT)
      Nebilet Plus
    • Slovenia (SI)
许可日期2009/01/20
最近更新日期2024/10/25
药物ATC编码
    • C07BB Beta blocking agents, selective, and thiazides
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
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