欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
LT/H/0108/001
药品名称
Etrixenal 250 mg tabletės
活性成分
naproxen 250.0 mg
剂型
Tablet
上市许可持有人
Proenzi s.r.o., Czech Republic
参考成员国 - 产品名称
Lithuania (LT)
Etrixenal 250mg tabletės
互认成员国 - 产品名称
Latvia (LV)
Etrixenal 250 mg tabletes
Hungary (HU)
ETRIXENAL 250 mg tabletta
Czechia (CZ)
Trebexen 250 mg tablety
Romania (RO)
Etrixenal 250 mg comprimate
许可日期
2014/08/14
最近更新日期
2023/01/25
药物ATC编码
M01AE02 naproxen
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:
Non Prescription (including OTC)
附件文件下载
Final Product Information
|
LT_108_IB_6_Etrixenal tab_naproxen_lab_en_PSUSA_CLEAN_181203_corrected
Date of last change:2024/09/06
Final Product Information
|
LT_108_IB_6_Etrixenal tab_naproxen_lab_en_PSUSA_tracked_181203_corrected___
Date of last change:2024/09/06
Final Product Information
|
LT_108_IB_6_Etrixenal tab_naproxen_PL_en_PSUSA_CLEAN_181203 _corrected
Date of last change:2024/09/06
Final Product Information
|
LT_108_IB_6_Etrixenal tab_naproxen_PL_en_PSUSA_track_181203_corrected
Date of last change:2024/09/06
Final Product Information
|
LT_108_IB_6_Etrixenal tab_naproxen_SPC_en_PSUSA_CLEAN_181203 _corrected
Date of last change:2024/09/06
Final Product Information
|
LT_108_IB_6_Etrixenal tab_naproxen_SPC_en_PSUSA_track_181203 _corrected
Date of last change:2024/09/06
Final Labelling
|
lt_h_0108_001_r_001_etrixenal_lab_en_2019_08_28_clean
Date of last change:2024/09/06
Final PL
|
lt_h_0108_001_r_001_etrixenal_pl_en_2019_08_28_clean
Date of last change:2024/09/06
Final PL
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lt_h_0108_001_r_001_etrixenal_pl_en_2019_08_28_track
Date of last change:2024/09/06
Final SPC
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lt_h_0108_001_r_001_etrixenal_spc_en_2019_08_28_clean
Date of last change:2024/09/06
Final SPC
|
lt_h_0108_001_r_001_etrixenal_spc_en_2019_08_28_track
Date of last change:2024/09/06
市场状态
Positive
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