欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）

MR编号	AT/H/0400/002
药品名称	Escitalopram +pharma 10 mg - Filmtabletten
活性成分	ESCITALOPRAM OXALATE 12.77 mg
剂型	Film-coated tablet
上市许可持有人	+pharma arzneimittel gmbh, Hafnerstraße 211, 8054 Graz, Österreich
参考成员国 - 产品名称	Austria (AT) Escitalopram +pharma 10 mg - Filmtabletten
互认成员国 - 产品名称	Poland (PL) Oroes Czechia (CZ) ESCITALOPRAM +PHARMA 10 MG
许可日期	2013/08/07
最近更新日期	2023/06/13
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 \| final_common_SPC_AT_H_0400_001-003_IB_014_cleanDate of last change:2021/04/19 Final PL \| final_common_PIL_AT_H_0400_001-003_IB_014_cleanDate of last change:2021/04/19 Final Labelling \| final_LAB_Escitalopram_20 mg_AT_H_400_003_R_002Date of last change:2020/06/05 Final Labelling \| final_LAB_Escitalopram_5 mg_AT_H_400_001_R_002Date of last change:2020/06/05 Final Labelling \| final_LAB_Escitalopram_10 mg_AT_H_400_002_R_002Date of last change:2020/06/05 PAR \| AT_H_0400_001-003_PAR_Escitalopram_+pharmaDate of last change:2016/07/18 Final Product Information \| final_LAB_Escitalopram_5mg_cleanDate of last change:2014/08/20 Final Product Information \| final_LAB_Escitalopram_10mg_cleanDate of last change:2014/08/20 Final Product Information \| final_LAB_Escitalopram_20mg_cleanDate of last change:2014/08/20 Final Product Information \| final_PL_Escitalopram_cleanDate of last change:2014/08/20 Final Product Information \| final_SmPC_Escitalopram_cleanDate of last change:2014/08/20
市场状态	Positive