欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/0198/001
药品名称
Celebra
活性成分
Celecoxib 100.0 mg
剂型
Capsule, hard
上市许可持有人
Upjohn EESV
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Germany (DE)
Celebrex 100/200 mg Filmtabletten
Denmark (DK)
Belgium (BE)
Netherlands (NL)
Celebrex 100 mg
Luxembourg (LU)
Celebrex
Iceland (IS)
United Kingdom (Northern Ireland) (XI)
Ireland (IE)
Austria (AT)
Celebrex 100 mg Hartkapseln
France (FR)
celebrex
Spain (ES)
Celebrex 100 mg, cápsulas duras
Portugal (PT)
Italy (IT)
Greece (GR)
Norway (NO)
Finland (FI)
Malta (MT)
Cyprus (CY)
40M0106
许可日期
2000/03/29
最近更新日期
2025/01/24
药物ATC编码
M01AH01 celecoxib
申请类型
TypeLevel1:
New Active Substance
TypeLevel2:
Initial Application
TypeLevel3:
Full Dossier Article 4.8 Di 65/65
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final PL
|
SE_H_0198_001_Final PL
Date of last change:2024/09/06
Final SPC
|
SE_H_0198_001_Final SPC
Date of last change:2024/09/06
市场状态
Positive
©2006-2025
Drugfuture
->
European Union HMA Authorisation of Medicines DataBase