欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/1076/002
药品名称
Celecoxib Upjohn
活性成分
Celecoxib 200.0 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
Netherlands (NL)
Celecoxib Viatris 200 mg harde capsules
United Kingdom (Northern Ireland) (XI)
Austria (AT)
Celecoxib Pfizer 200 mg Hartkapseln
Italy (IT)
Finland (FI)
许可日期
2012/01/26
最近更新日期
2025/01/24
药物ATC编码
M01AH01 celecoxib
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
Final PL
|
SE_H_1076_002_Final PL
Date of last change:2024/09/06
Final SPC
|
SE_H_1076_002_Final SPC
Date of last change:2024/09/06
PubAR
|
SE_H_1076_002_PAR
Date of last change:2024/09/06
市场状态
Positive
©2006-2025
Drugfuture
->
European Union HMA Authorisation of Medicines DataBase