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)
Slovakia (SK)
许可日期
2002/11/21
最近更新日期
2024/09/26
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 SPC
|
11836_300 mg_Renewal FINAL SPC
Date of last change:2024/09/06
Final Product Information
|
1b_spc_pl_prilium150mg_en_clean_version
Date of last change:2024/09/06
Final Product Information
|
1b_spc_pl_prilium300mg_en_clean_version
Date of last change:2024/09/06
Final Product Information
|
1b_spc_pl_prilium75mg_en_clean_version
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase