欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/4650/001
药品名称Oxycodon/Naloxon G.L. 5 mg/2,5 mg Retardtabletten
活性成分
    • NALOXONE HYDROCHLORIDE dihydrate 2.75 mg
    • oxycodone hydrochloride 5.0 mg
剂型Prolonged-release tablet
上市许可持有人G.L. Pharma GmbH Schlossplatz 1 8502 LANNACH Österreich
参考成员国 - 产品名称Germany (DE)
Oxycodon Naloxon G.L. 5/2,5 mg Retardtabletten
互认成员国 - 产品名称
    • Austria (AT)
      Oxylanox 5 mg/2,5 mg-Retardtabletten
    • Sweden (SE)
    • Poland (PL)
      Oxylaxon
    • Latvia (LV)
      Geroxynal 5 mg /2,5 mg ilgstošās darbības tabletes
    • Lithuania (LT)
      Oxycodone / Naloxone G.L. Pharma 5 mg / 2,5 mg pailginto atpalaidavimo tabletės
    • Estonia (EE)
      GEROXYNAL
    • Slovakia (SK)
      Oxykodón/Naloxón G.L. Pharma 5 mg/2,5 mg tablety s predĺženým uvoľňovaním
许可日期2017/08/10
最近更新日期2024/03/13
药物ATC编码
    • N02AA55 oxycodone and naloxone
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