欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
NL/H/1732/003
药品名称
Zoloft 100
活性成分
sertraline 100.0 mg
剂型
Film-coated tablet
上市许可持有人
Pfizer BV Capelle a/d IJssel The Netherlands Former RMS SE/H/937/01
参考成员国 - 产品名称
Netherlands (NL)
互认成员国 - 产品名称
Germany (DE)
Denmark (DK)
Belgium (BE)
Luxembourg (LU)
Iceland (IS)
United Kingdom (Northern Ireland) (XI)
Ireland (IE)
Spain (ES)
Portugal (PT)
Italy (IT)
Greece (GR)
Sweden (SE)
Norway (NO)
Finland (FI)
Poland (PL)
Zoloft
Cyprus (CY)
Czechia (CZ)
Romania (RO)
Zoloft 100 mg comprimate filmate
Slovenia (SI)
Slovakia (SK)
Austria (AT)
Tresleen 100 mg Filmtabletten
许可日期
2009/09/28
最近更新日期
2024/02/13
药物ATC编码
N06AB06 sertraline
申请类型
TypeLevel1:
[not specified]
TypeLevel2:
[not specified]
TypeLevel3:
[not specified]
TypeLevel4:
[not specified]
TypeLevel5:
[not specified]
附件文件下载
Final PL
|
PIL
Date of last change:2024/02/13
Final Labelling
|
common-outer-label-zoloft-sertraline-25mg-50mg-100mg-fct20mg-ml-oral-solution-clean
Date of last change:2019/02/12
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase