欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号AT/H/0598/001
药品名称Ulcamed 120 mg Filmtabletten
活性成分
    • bismuth subcitrate 120.0 mg
剂型Film-coated tablet
上市许可持有人Krka, d.d., Novo mesto, Šmarješka cesta 6, 8501 Novo mesto, Slovenia
参考成员国 - 产品名称Austria (AT)
Ulcamed 120 mg Filmtabletten
互认成员国 - 产品名称
    • Greece (GR)
    • Lithuania (LT)
      Ulcamed 120 mg plėvele dengtos tabletės
    • Estonia (EE)
      ULCAMED
    • Bulgaria (BG)
      Ulcamed
    • Czechia (CZ)
      Ulcamed
    • Poland (PL)
      Ulcamed
    • Hungary (HU)
      Ulcamed 120 mg filmtabletta
    • Romania (RO)
      Ulcamed 120 mg comprimate filmate
    • Slovakia (SK)
      Ulcamed 120 mg filmom obalené tablety
    • Slovenia (SI)
    • Croatia (HR)
      Ulcamed 120 mg filmom obložene tablete
许可日期2015/10/02
最近更新日期2021/12/14
药物ATC编码
    • A02BX05 bismuth subcitrate
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Bibliographic Art 10 a 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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