欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/1115/001
药品名称Belfor 20 mg/5 mg
活性成分
    • amlodipine 5.0 mg
    • olmesartan medoxomil 20.0 mg
剂型Film-coated tablet
上市许可持有人Menarini International O.L. S.A. 1, Avenue de la Gare L-1611 Luxembourg
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    • Germany (DE)
      Votamax 20 mg/5 mg Filmtabletten
    • Belgium (BE)
    • Luxembourg (LU)
    • Ireland (IE)
    • Austria (AT)
      Amelior 20 mg/5 mg Filmtabletten
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
      Zolnor
    • Italy (IT)
    • Greece (GR)
    • Poland (PL)
      Elestar
    • Latvia (LV)
    • Lithuania (LT)
      Sanoral 20 mg/5 mg plėvele dengtos tabletės
    • Estonia (EE)
      SANORAL
    • Hungary (HU)
      DUACTAN 20 mg/5 mg filmtabletta
    • Bulgaria (BG)
      Tespadan
    • Cyprus (CY)
      orizal 20mg/5mg f.c tabs
    • Czechia (CZ)
    • Romania (RO)
      Inovum 20 mg/5 mg, comprimate filmate
    • Slovakia (SK)
      Folgan 20 mg / 5 mg
    • Slovenia (SI)
    • Malta (MT)
      Tansar 20mg/5mg
许可日期2008/07/30
最近更新日期2024/04/02
药物ATC编码
    • C09D ANGIOTENSIN II RECEPTOR BLOCKERS (ARBs), COMBINATIONS
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Multiple (Copy) 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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