欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
HU/H/0179/002
药品名称
Escitalopram-Vera
活性成分
Escitalopram oxalate 10.0 mg
剂型
Film-coated tablet
上市许可持有人
TEVA Gyógyszergyár ZRt.
参考成员国 - 产品名称
Hungary (HU)
ESCITALOPRAM-TEVA 10 mg filmtabletta
互认成员国 - 产品名称
Denmark (DK)
Ireland (IE)
Estonia (EE)
Slovenia (SI)
Germany (DE)
Escitalopram-ratiopharm 10 mg Filmtabletten
Belgium (BE)
Netherlands (NL)
Luxembourg (LU)
United Kingdom (Northern Ireland) (XI)
France (FR)
Italy (IT)
Sweden (SE)
Portugal (PT)
Lithuania (LT)
Escitalopram Teva 10mg plėvele dengtos tabletės
Czechia (CZ)
Slovakia (SK)
许可日期
2008/12/28
最近更新日期
2025/01/14
药物ATC编码
N06AB10 escitalopram
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Initial Application
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 SPC
|
HU_H_0179_001_004_WS_063_Escitalopram_FINAL_SmPC_Clean
Date of last change:2025/01/14
Final PL
|
HU_H_0179_001_004_WS_063_Escitalopram_FINAL_PIL_Clean
Date of last change:2025/01/14
PubAR
|
EscitalopramTeva_PAReng
Date of last change:2024/09/06
市场状态
Positive
©2006-2025
Drugfuture
->
European Union HMA Authorisation of Medicines DataBase