欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
EE/H/0360/003
药品名称
Lisinopril Grindeks
活性成分
lisinopril 20.0 mg
剂型
Tablet
上市许可持有人
Grindeks AS Krustpils Iela 53 Riga 1057 Latvia
参考成员国 - 产品名称
Estonia (EE)
互认成员国 - 产品名称
Austria (AT)
France (FR)
Spain (ES)
Portugal (PT)
Italy (IT)
Greece (GR)
Finland (FI)
Poland (PL)
Hungary (HU)
Bulgaria (BG)
Lisinopril Baltijos Bite
Belgium (BE)
Romania (RO)
Ireland (IE)
Slovakia (SK)
许可日期
2023/01/18
最近更新日期
2023/01/18
药物ATC编码
C09AA03 lisinopril
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Additional Strength/Form
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 Labelling
|
Lisinopril_labelling_common_clean
Date of last change:2024/09/06
Final PL
|
Lisinopril_PIL_common_D201_clean_09_01_2023
Date of last change:2024/09/06
Final SPC
|
Lisinopril_SPC_common_D195_IE__clean_02_01_2023
Date of last change:2024/09/06
PubAR
|
Public AR_EE_H_0360_DC
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase