欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/4650/005
药品名称Oxycodon/Naloxon G.L. 40 mg/20 mg Retardtabletten
活性成分
    • NALOXONE HYDROCHLORIDE dihydrate 21.98 mg
    • oxycodone hydrochloride 40.0 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. 40/20 mg Retardtabletten
互认成员国 - 产品名称
    • Austria (AT)
      Oxylanox 40 mg/20 mg-Retardtabletten
    • Sweden (SE)
    • Poland (PL)
      Oxylaxon
    • Latvia (LV)
      Geroxynal 40 mg/20 mg ilgstošās darbības tabletes
    • Lithuania (LT)
      Oxycodone / Naloxone G.L. Pharma 40 mg / 20 mg pailginto atpalaidavimo tabletės
    • Estonia (EE)
      GEROXYNAL
    • Czechia (CZ)
    • Slovakia (SK)
      Oxykodón/Naloxón G.L. Pharma 40 mg/20 mg tablety s predĺženým uvoľňovaním
许可日期2017/08/10
最近更新日期2024/04/17
药物ATC编码
    • N02AA55 oxycodone and naloxone
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Additional Strength/Form
  • 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
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