欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
SE/H/2239/001
药品名称
Escitalopram Grindeks
活性成分
escitalopram oxalate 5.0 mg
剂型
Film-coated tablet
上市许可持有人
Grindeks AS
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Romania (RO)
Portugal (PT)
Slovakia (SK)
Italy (IT)
Slovenia (SI)
Greece (GR)
Croatia (HR)
Norway (NO)
Germany (DE)
Escitalopram Grindeks 5 mg Filmtabletten
Poland (PL)
Escitalopram Grindeks
Belgium (BE)
Latvia (LV)
Netherlands (NL)
Lithuania (LT)
Escitalopram Grindeks 5 mg plėvele dengtos tabletės
Luxembourg (LU)
Estonia (EE)
Ireland (IE)
Hungary (HU)
Escitalopram Grindeks
Austria (AT)
Bulgaria (BG)
Escitalopram Grindeks
France (FR)
Czechia (CZ)
Escitalopram Grindeks
Spain (ES)
许可日期
2023/05/17
最近更新日期
2023/06/19
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 PL
|
Final PL
Date of last change:2024/09/06
Final SPC
|
Final SPC
Date of last change:2024/09/06
PubAR
|
https___www_lakemedelsverket_se_sv_sok_lakemedelsfakta_lakemedel_id_20211230000010
Date of last change:2024/09/06
PubAR Summary
|
https___www_lakemedelsverket_se_sv_sok_lakemedelsfakta_lakemedel_id_20211230000010_2
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase