欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/0278/001
药品名称
Cipralex
活性成分
Escitalopram 5.0 mg
剂型
Film-coated tablet
上市许可持有人
H. Lundbeck A/S Denmark
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Latvia (LV)
Denmark (DK)
Belgium (BE)
Luxembourg (LU)
Iceland (IS)
United Kingdom (Northern Ireland) (XI)
Ireland (IE)
Austria (AT)
Cipralex 5 mg - Filmtabletten
France (FR)
Spain (ES)
Italy (IT)
Greece (GR)
Norway (NO)
Finland (FI)
Cyprus (CY)
Malta (MT)
Portugal (PT)
许可日期
2002/05/07
最近更新日期
2024/11/27
药物ATC编码
N06AB10 escitalopram
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_0278_001_Final PL
Date of last change:2024/09/06
Final SPC
|
SE_H_0278_001_Final SPC
Date of last change:2024/09/06
PubAR
|
SE_H_0278_001_PAR
Date of last change:2024/09/06
市场状态
Positive
©2006-2025
Drugfuture
->
European Union HMA Authorisation of Medicines DataBase