欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/4510/001
药品名称Refero
活性成分
    • rifaximin 550.0 mg
剂型Film-coated tablet
上市许可持有人Alfasigma S.p.A. Via Ragazzi del ’99, n.5 40133 Bologna (BO) Italy
参考成员国 - 产品名称Netherlands (NL)
TIXTELLER 550 mg filmomhulde tabletten
互认成员国 - 产品名称
    • Germany (DE)
      REFERO Filmtabletten
    • Belgium (BE)
      Tixteller
    • Luxembourg (LU)
    • Ireland (IE)
    • Austria (AT)
      Refero 550 mg Filmtabletten
    • Portugal (PT)
    • Italy (IT)
    • Poland (PL)
      Tixteller
    • Hungary (HU)
      REFERO 550 mg filmtabletta
    • Romania (RO)
      Tixteller 550 mg comprimate filmate
    • Slovakia (SK)
    • Spain (ES)
    • France (FR)
许可日期2012/11/29
最近更新日期2024/07/02
药物ATC编码
    • A07AA11 rifaximin
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
©2006-2024 Drugfuture->European Union HMA Authorisation of Medicines DataBase