欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/1158/001
药品名称
Vancomycin Mylan
活性成分
vancomycin hydrochloride 500.0 mg
剂型
Powder for solution for infusion
上市许可持有人
Mylan Ireland Limited
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Lithuania (LT)
Vancomycin Mylan 500 mg milteliai infuzinio tirpalo koncentratui
Romania (RO)
Vancomicina Mylan 500 mg pulbere pentru concentrat pentru soluţie perfuzabilă
Slovenia (SI)
Vankomicin FarmaPlus 500 mg prašek za koncentrat za raztopino za infundiranje
United Kingdom (Northern Ireland) (XI)
France (FR)
Norway (NO)
许可日期
2012/11/12
最近更新日期
2022/03/04
药物ATC编码
J01XA01 vancomycin
申请类型
TypeLevel1:
Known Active Substance
TypeLevel2:
Initial Application
TypeLevel3:
Bibliographic Art 10 a Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final PL
|
SE/H/1158/001_Final PL
Date of last change:2014/01/15
Final SPC
|
SE/H/1158/001_Final SPC
Date of last change:2014/01/15
PAR
|
SE/H/1158/001_PAR
Date of last change:2014/01/15
市场状态
Positive
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