欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
FR/V/0133/003
药品名称
PRILIUM 300 MG
活性成分
imidapril hydrochloride 300.0 mg
剂型
Powder for oral solution
上市许可持有人
VETOQUINOL SA MAGNY-VERNOIS 70204 LURE CEDEX FRANCE
参考成员国 - 产品名称
France (FR)
互认成员国 - 产品名称
Germany (DE)
Denmark (DK)
Belgium (BE)
Luxembourg (LU)
Austria (AT)
Italy (IT)
Greece (GR)
Finland (FI)
Poland (PL)
Hungary (HU)
Czechia (CZ)
Slovakia (SK)
许可日期
2002/11/21
最近更新日期
2022/04/15
药物ATC编码
QC09AA16 imidapril
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 Product Information
|
1b-spc-pl-prilium150mg-en-clean-version
Date of last change:2021/02/12
Final Product Information
|
1b-spc-pl-prilium300mg-en-clean-version
Date of last change:2021/02/12
Final Product Information
|
1b-spc-pl-prilium75mg-en-clean-version
Date of last change:2021/02/12
Final SPC
|
11836-300 mg-Renewal FINAL SPC
Date of last change:2012/05/04
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase