欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
SE/H/1158/002
药品名称
Vancomycin Mylan
活性成分
Vancomycin hydrochloride 1000.0 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
United Kingdom (Northern Ireland) (XI)
France (FR)
Norway (NO)
Latvia (LV)
Vancomycin FarmaPlus 1000 mg pulveris infūziju šķīduma koncentrāta pagatavošanai
Lithuania (LT)
Vancomycin Mylan 1000 mg milteliai infuzinio tirpalo koncentratui
Romania (RO)
Vancomicina Mylan 1000 mg pulbere pentru concentrat pentru soluţie perfuzabilă
Slovenia (SI)
Vankomicin FarmaPlus 1000 mg prašek za koncentrat za raztopino za infundiranje
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：
Additional Strength/Form
TypeLevel3：
Bibliographic
TypeLevel4：
Chemical Substance
TypeLevel5：
Prescription Only
附件文件下载
Final PL
|
SE_H_1158_002_Final PL
Date of last change:2024/09/06
Final SPC
|
SE_H_1158_002_Final SPC
Date of last change:2024/09/06
PubAR
|
SE_H_1158_002_PAR
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase