欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/0198/002
药品名称
Celebra
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
Malta (MT)
Cyprus (CY)
CELEBREX 200MG, HARD CAPSULE
Finland (FI)
Norway (NO)
Greece (GR)
Italy (IT)
Portugal (PT)
Spain (ES)
Celebrex 200 mg, cápsulas duras
France (FR)
Celebrex
Austria (AT)
Celebrex 200 mg Hartkapseln
Ireland (IE)
United Kingdom (Northern Ireland) (XI)
Germany (DE)
Celebrex 100/200 mg Filmtabletten
Luxembourg (LU)
Celebrex
Iceland (IS)
Netherlands (NL)
Celebrex 200 mg
Belgium (BE)
Denmark (DK)
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:
Additional Strength/Form
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_002_Final PL
Date of last change:2024/09/06
Final SPC
|
SE_H_0198_002_Final SPC
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase