欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号FR/H/7500/001
药品名称Daflon 500 mg
活性成分
    • diosmin 450.0 mg
    • HESPERIDIN 50.0 mg
剂型Film-coated tablet
上市许可持有人SERVIER
参考成员国 - 产品名称France (FR)
EUDION 500MG, comprimé pelliculé
互认成员国 - 产品名称
    • Denmark (DK)
      Capiven
    • Belgium (BE)
      DAFLON 500mg comprimés pelliculés
    • Luxembourg (LU)
      DAFLON 500 mg comprimés pelliculés
    • Austria (AT)
      Daflon 500 mg - Filmtabletten
    • Spain (ES)
      DAFLON 500, comprimidos recubiertos
    • Portugal (PT)
      DAFLON 500
    • Italy (IT)
      ARVENUM 500 mg compresse rivestite con film
    • Greece (GR)
      DAFLON 500 mg, επικαλυμμένο με λεπτό υμένιο δισκίο
    • Latvia (LV)
      Detralex 500mg apvalkotās tabletes
    • Lithuania (LT)
      Detralex 500 mg plėvele dengtos tabletės
    • Hungary (HU)
      Detralex 500 mg filmtabletta
    • Bulgaria (BG)
      ДЕТРАЛЕКС 500 mg филмирани таблетки
    • Czechia (CZ)
      DETRALEX 500 mg potahované tablety
    • Romania (RO)
      DETRALEX 500 mg comprimate filmate
    • Slovakia (SK)
      DETRALEX
    • Slovenia (SI)
      DETRALEX filmsko obložene tablete
    • Malta (MT)
      DAFLON 500 mg, film-coated tablet
    • Croatia (HR)
      DETRALEX 500 mg filmom obložene tablete
许可日期2018/05/26
最近更新日期2019/01/02
药物ATC编码
    • C05CA53 diosmin, combinations
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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