欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/1339/001
药品名称
Meropenem Aurovitas
活性成分
Meropenem trihydrate 500.0 mg
剂型
Powder for solution for infusion/injection
上市许可持有人
Aurovitas Unipessoal, Lda.
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Germany (DE)
Meropenem PUREN 500 mg Pulver zur Herstellung einer Injektions-/Infusionslösung
Belgium (BE)
Meropenem Eugia 500 mg poeder voor oplossing voor injectie/infusie
Ireland (IE)
Spain (ES)
Italy (IT)
许可日期
2015/10/28
最近更新日期
2024/12/19
药物ATC编码
J01DH02 meropenem
申请类型
TypeLevel1:
Abridged
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
PubAR
|
590547_590548_20160120_PAR_RCM
Date of last change:2024/09/06
Final PL
|
common_pl_clean
Date of last change:2024/09/06
Final SPC
|
common_spc_clean
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase