欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/0461/004
药品名称
Cefuroxima Aurobindo
活性成分
Cefuroximaxetil 250.0 mg
剂型
Film-coated tablet
上市许可持有人
Aurobindo Pharma (Portugal), Unipessoal Lda
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Germany (DE)
Cefuroxim Aurobindo 250 mg Filmtabletten
Ireland (IE)
Spain (ES)
Romania (RO)
Cefuroxima AUROBINDO 250 mg comprimate filmate
许可日期
2015/08/05
最近更新日期
2024/10/28
药物ATC编码
J01DC02 cefuroxime
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
Final SPC
|
common_spc
Date of last change:2024/11/09
Final PL
|
common_pl
Date of last change:2024/10/28
市场状态
Positive
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