欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/0818/001
药品名称
Citalopram Vitabalans
活性成分
citalopram hydrobromide 20.0 mg
剂型
Film-coated tablet
上市许可持有人
Vitabalans Oy, Finland
参考成员国 - 产品名称
Sweden (SE)
Citalopram Vitabalans
互认成员国 - 产品名称
Germany (DE)
CITALOTIN 20 mg Filmtabletten
Denmark (DK)
Norway (NO)
Finland (FI)
Poland (PL)
Citalopram Vitabalans
Latvia (LV)
Lithuania (LT)
Citalopram Vitabalans 20 mg plėvele dengtos tabletės
Estonia (EE)
CITALOPRAM VITABALANS
Hungary (HU)
CITALOPRAM VITABALANS 20 mg filmtabletta
Czechia (CZ)
CITALOTIN 20 mg Potahované tablety
Slovakia (SK)
CITALONIN 20 mg filmom obalené tablety
Slovenia (SI)
Citalopram Vitablans 20 mg filmsko obložene tablete
许可日期
2010/11/19
最近更新日期
2024/04/11
药物ATC编码
N06AB04 citalopram
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
|
SE/H/0818/001_Final PL
Date of last change:2014/01/15
Final SPC
|
SE/H/0818/001_Final SPC
Date of last change:2014/01/15
PAR
|
SE/H/0818/001_PAR
Date of last change:2014/01/15
市场状态
Positive
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