欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/7732/002
药品名称Celecoxib 200 mg hard capsules
活性成分
    • Celecoxib 200.0 mg
剂型Capsule, hard
上市许可持有人ratiopharm GmbH Graf-Arco-Str. 3 89079 Ulm Germany
参考成员国 - 产品名称Germany (DE)
Celecoxib-ratiopharm 200 mg Hartkapseln
互认成员国 - 产品名称
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Romania (RO)
    • Croatia (HR)
    • Belgium (BE)
      Celecoxib Teva Generics 200 mg harde capsules
    • Netherlands (NL)
    • Iceland (IS)
    • Austria (AT)
许可日期2024/11/14
最近更新日期2024/11/25
药物ATC编码
    • M01AH01 celecoxib
申请类型
  • TypeLevel1:Known Active Substance
  • 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
©2006-2025 Drugfuture->European Union HMA Authorisation of Medicines DataBase