欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/1151/001
药品名称Naltrexone Hydrochloride Accord 50 mg filmcoated tablets
活性成分
    • naltrexone hydrochloride 50.0 mg
剂型Film-coated tablet
上市许可持有人Accord Healthcare B.V. Winthontlaan 200 3526 KV UTRECHT
参考成员国 - 产品名称Netherlands (NL)
RVG 102900
互认成员国 - 产品名称
    • Austria (AT)
    • Cyprus (CY)
    • Denmark (DK)
      Naltrexone Hydrochlorid Accord
    • Belgium (BE)
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
    • Spain (ES)
    • Portugal (PT)
      Naltrexona Accord
    • Italy (IT)
    • Finland (FI)
    • Poland (PL)
      Naltrexone Hydrochloride Accord
    • Latvia (LV)
      Naltrexone Accord 50 mg apvalkotās tabletes
    • Lithuania (LT)
      Naltrexone Accord 50 mg plėvele dengtos tabletės
    • Estonia (EE)
      NALTREXONE ACCORD
    • Germany (DE)
    • Sweden (SE)
    • Norway (NO)
许可日期2010/02/04
最近更新日期2024/02/02
药物ATC编码
    • N07BB04 naltrexone
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Initial Application
  • TypeLevel3:Generic Art 10.1 and 10.2 Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
附件文件下载
市场状态Positive
©2006-2024 Drugfuture->European Union HMA Authorisation of Medicines DataBase