欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
IT/H/0808/002
药品名称
CELARTROX
活性成分
celecoxib 200.0 mg
剂型
Capsule, hard
上市许可持有人
SF Group srl Via Tiburtina 1143 00156 Roma Italy
参考成员国 - 产品名称
Italy (IT)
互认成员国 - 产品名称
许可日期
2014/03/20
最近更新日期
2022/01/20
药物ATC编码
M01AH01 celecoxib
申请类型
TypeLevel1:
[not specified]
TypeLevel2:
[not specified]
TypeLevel3:
[not specified]
TypeLevel4:
[not specified]
TypeLevel5:
[not specified]
附件文件下载
Final Labelling
|
2257 outer_celecoxib_DK_H_2257_01_P001_v1_1_100418_CL
Date of last change:2024/09/06
Final Labelling
|
2257 outer_celecoxib_DK_H_2257_02_P001_v1_1_100418_CL
Date of last change:2024/09/06
Final SPC
|
PIL_celecoxib_DK_H_2257_01_02_v2_2 CL_27032019
Date of last change:2024/09/06
Final PL
|
PIL_celecoxib_DK_H_2257_01_02_v2_2 CL_27032019_2
Date of last change:2024/09/06
PubAR
|
Sigcelox 2257 Final PAR
Date of last change:2024/09/06
Final Product Information
|
SmPC_celecoxib_DK_H_2257_01_02_V011_v2_1_161116_CL
Date of last change:2024/09/06
Final SPC
|
SmPC_celecoxib_DK_H_2257_01_02_v3_3 CL_150519
Date of last change:2024/09/06
Final Product Information
|
SmPC_celecoxib_DK_H_2261_01_02_V012_v2_1_161116_CL
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase