欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
IE/H/0452/003
药品名称
Eprosartan Teva
活性成分
eprosartan 600.0 mg
剂型
Film-coated tablet
上市许可持有人
Teva B.V., Swensweg 5, 2031GA Haarlem, Netherlands
参考成员国 - 产品名称
Ireland (IE)
互认成员国 - 产品名称
United Kingdom (Northern Ireland) (XI)
许可日期
2015/01/23
最近更新日期
2021/01/05
药物ATC编码
C09CA02 eprosartan
申请类型
TypeLevel1：
Known Active Substance
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 Product Information
|
im pack, 300, 400, 600mg
Date of last change:2015/03/10
Final Product Information
|
common-outer-clean
Date of last change:2015/03/10
Final Product Information
|
common-outer-tracked
Date of last change:2015/03/10
Final Product Information
|
common-pl-clean
Date of last change:2015/03/10
Final Product Information
|
common-pl-tracked
Date of last change:2015/03/10
Final Product Information
|
common-spc-clean
Date of last change:2015/03/10
Final Product Information
|
common-spc-tracked
Date of last change:2015/03/10
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase