欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/0339/001
药品名称
Vancomicina Hikma
活性成分
vancomycin hydrochloride 500.0 mg
剂型
Powder for solution for infusion
上市许可持有人
Hikma Farmacêutica (Portugal), S.A.
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Romania (RO)
Slovakia (SK)
Hungary (HU)
VANCOMYCIN PHARMASWISS 500 mg por oldatos infúzióhoz
许可日期
2010/07/14
最近更新日期
2024/03/06
药物ATC编码
J01XA01 vancomycin
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 Product Information
|
common-outer-500mg1000mg-clean
Date of last change:2014/10/31
Final Product Information
|
common-pl-500mg1000mg-clean
Date of last change:2014/10/31
Final Product Information
|
common-spc-500mg1000mg-clean
Date of last change:2014/10/31
市场状态
Positive
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