欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DK/H/0314/004
药品名称
Lisinopril "Actavis"
活性成分
lisinopril dihydrate 20.0 mg
剂型
Tablet
上市许可持有人
Actavis Nordic A/S Ørnegårdsvej 16 DK-2820 Gentofte Denmark
参考成员国 - 产品名称
Denmark (DK)
互认成员国 - 产品名称
Sweden (SE)
许可日期
2002/02/13
最近更新日期
2023/08/18
药物ATC编码
C09AA03 lisinopril
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Additional Strength/Form
TypeLevel3:
Generic Article 4.8(a)(iii), first paragraph
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final Labelling
|
Lisinopril_DK_H_0314_002_004_ImP Bottle_25_02_19
Date of last change:2024/09/06
Final Labelling
|
Lisinopril_DK_H_0314_002_004_OuP_25_02_19
Date of last change:2024/09/06
Final PL
|
Lisinopril_DK_H_0314_002_004_PIL_13_04_23_tracked
Date of last change:2024/09/06
Final SPC
|
Lisinopril_DK_H_0314_002_004_SPC_13_04_23_clean
Date of last change:2024/09/06
Final Product Information
|
PI_Lisinopril_DK_H_0314_02_04_V044_v3_1_280416_CLEAN
Date of last change:2024/09/06
市场状态
Positive
©2006-2024
Drugfuture
->
European Union HMA Authorisation of Medicines DataBase