欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号FR/V/0282/001
药品名称NEOMAY 500 mg/g
活性成分
    • neomycin 50.0 %
剂型Powder for oral solution
上市许可持有人Laboratorios Maymó
参考成员国 - 产品名称France (FR)
13830
互认成员国 - 产品名称
    • Denmark (DK)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
      Neomay 500 IU/g Powder for use in drinking water/milk
    • Greece (GR)
    • Hungary (HU)
    • Poland (PL)
    • Czechia (CZ)
      NEOMAY 500 000 IU/g prášek pro podání v pitné vodě/mléčné náhražce
    • Romania (RO)
    • Slovenia (SI)
    • Slovakia (SK)
    • Croatia (HR)
许可日期2015/09/23
最近更新日期2022/11/23
药物ATC编码
    • QA07AA01 neomycin
申请类型
  • TypeLevel1:[not specified]
  • TypeLevel2:[not specified]
  • TypeLevel3:Other Generic application Art 13.3 Dir 2001/82/EC
  • 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