欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DK/H/0752/003
药品名称
Loxopram
活性成分
citalopram hydrobromide 40.0 mg
剂型
Film-coated tablet
上市许可持有人
Ratiopharm GmbH Graf-Arco-Str. 3 89079 Ulm Germany
参考成员国 - 产品名称
Denmark (DK)
互认成员国 - 产品名称
Austria (AT)
Citalopram "ratiopharm" 40 mg-Filmtabletten
许可日期
2005/06/08
最近更新日期
2024/04/04
药物ATC编码
N06AB04 citalopram
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Additional Strength/Form
TypeLevel3:
Generic [Article 10.1.(a)(iii), first paragraph]
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final PL
|
Citalopram_DK_H_0752_001_003_PIL_02_01_24
Date of last change:2024/04/04
Final SPC
|
Citalopram_DK_H_0752_001_003_SmPC_02_01_24
Date of last change:2024/04/04
Final Labelling
|
Citalopram-DK_H_0752_001-003-OuP+ImP%20(Label+Blister)
Date of last change:2021/06/16
Final Product Information
|
common-spc-clean
Date of last change:2013/01/29
Final Product Information
|
common-pl-clean
Date of last change:2013/01/29
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase