欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PL/H/0431/001
药品名称
Ezetimibe Adamed
活性成分
Ezetimibe 10.0 mg
剂型
Tablet
上市许可持有人
Adamed Sp. z o.o. Pienkow 149 05-152 Czosnow Poland
参考成员国 - 产品名称
Poland (PL)
Ezehron
互认成员国 - 产品名称
Austria (AT)
Ezetimib Genericon 10 mg Tabletten
Greece (GR)
EZETIMIBE/ADAMED
Hungary (HU)
NOXETIB 10 mg tabletta
Bulgaria (BG)
Езетимиб Адамед 10 mg таблетки
许可日期
2017/05/09
最近更新日期
2024/10/08
药物ATC编码
C10AX09 ezetimibe
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
|
2020_09 Ezetimibe Adamed tablet ENG PL_track
Date of last change:2024/09/06
Final Product Information
|
common _ LAB_clean_04_2017
Date of last change:2024/09/06
Final Product Information
|
common _ LAB_track_04_2017
Date of last change:2024/09/06
Final Product Information
|
common _ PIL_clean_04_2017
Date of last change:2024/09/06
Final Product Information
|
common _ PIL_track_04_2017
Date of last change:2024/09/06
Final Product Information
|
common _ SPC_clean_04_2017
Date of last change:2024/09/06
Final Product Information
|
common _ SPC_track_04_2017
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase