欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PL/H/0685/001
药品名称
Agregex
活性成分
clopidogrel bisulfate 75.0 mg
剂型
Film-coated tablet
上市许可持有人
Actavis Group PTC ehf. Reykjavikurvegur 76-78, 220 Hafnarfjödur Iceland
参考成员国 - 产品名称
Poland (PL)
互认成员国 - 产品名称
Cyprus (CY)
AGREGEX 75mg FC TABS
Malta (MT)
许可日期
2009/10/01
最近更新日期
2023/10/04
药物ATC编码
B01AC04 clopidogrel
B01AC Platelet aggregation inhibitors excl. heparin
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 Labelling
|
Clopidogrel_DK H_1624_001_OuP_ImP _blister__23_04_19_CLEAN
Date of last change:2024/09/06
Final Labelling
|
Clopidogrel_DK H_1624_001_OuP_ImP _bottle__23_04_19_CLEAN
Date of last change:2024/09/06
Final Product Information
|
Clopidogrel_DK H_1624_001_PI_19_07_18 CL
Date of last change:2024/09/06
Final SPC
|
Clopidogrel_DK H_1624_001_PIL_12_06_19_CLEAN
Date of last change:2024/09/06
Final PL
|
Clopidogrel_DK H_1624_001_PIL_23_04_19_CLEAN
Date of last change:2024/09/06
Final SPC
|
Clopidogrel_DK H_1624_001_SmPC_12_06_19_CLEAN
Date of last change:2024/09/06
PubAR
|
parmod5_dk1624agregex_pdf
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase