欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
SE/H/2239/003
药品名称
Escitalopram Grindeks
活性成分
escitalopram oxalate 20.0 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 20 mg Filmtabletten
Poland (PL)
Escitalopram Grindeks
Belgium (BE)
Latvia (LV)
Netherlands (NL)
Lithuania (LT)
Escitalopram Grindeks 20 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：
Additional Strength/Form
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_20211230000034
Date of last change:2024/09/06
PubAR Summary
|
https___www_lakemedelsverket_se_sv_sok_lakemedelsfakta_lakemedel_id_20211230000034_2
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase