欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/2020/009
药品名称Palexia retard
活性成分
    • tapentadol hydrochloride 29.12 mg
剂型Prolonged-release tablet
上市许可持有人Grünenthal GmbH Zieglerstrasse 6 D- 52078 Aachen Germany
参考成员国 - 产品名称Germany (DE)
Palexia retard 25 mg
互认成员国 - 产品名称
    • Slovakia (SK)
      Palexia retard 25 mg tablety s predľženým uvoľňovaním
    • Slovenia (SI)
      Palexia SR 25 mg tablete s podaljšanim sproscanjem
    • Croatia (HR)
      Palexia retard 25 mg tablete s produljenim oslobađanjem
    • Netherlands (NL)
    • Denmark (DK)
      Palexia Depot
    • Belgium (BE)
    • Luxembourg (LU)
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Sweden (SE)
    • Norway (NO)
    • Poland (PL)
      Palexia retard
    • Cyprus (CY)
      PALEXIA 25mg PR TABS
许可日期2012/03/29
最近更新日期2024/10/21
药物ATC编码
    • N02AX06 tapentadol
申请类型
  • TypeLevel1:Line Extension
  • TypeLevel2:Additional Strength/Form
  • TypeLevel3:Full Dossier Art 8.3(i) 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