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
United Kingdom (Northern Ireland) (XI)
Ireland (IE)
Austria (AT)
Celebrex 200 mg Hartkapseln
France (FR)
Celebrex
Spain (ES)
Celebrex 200 mg, cápsulas duras
Portugal (PT)
Italy (IT)
Greece (GR)
Norway (NO)
Finland (FI)
Cyprus (CY)
CELEBREX 200MG, HARD CAPSULE
Malta (MT)
Germany (DE)
Celebrex 100/200 mg Filmtabletten
Denmark (DK)
Belgium (BE)
Netherlands (NL)
Celebrex 200 mg
Luxembourg (LU)
Celebrex
Iceland (IS)
许可日期
2000/03/29
最近更新日期
2024/01/16
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:2014/01/15
Final SPC
|
SE/H/0198/002_Final SPC
Date of last change:2014/01/15
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase