欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/1245/001
药品名称
Linezolida Glenmark
活性成分
linezolid 600.0 mg
剂型
Film-coated tablet
上市许可持有人
Glenmark Pharmaceuticals Europe Ltd
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
France (FR)
Germany (DE)
Linezolid Glenmark 600 mg Filmtabletten
Denmark (DK)
United Kingdom (Northern Ireland) (XI)
Spain (ES)
Italy (IT)
Sweden (SE)
Poland (PL)
Dilizolen
许可日期
2015/08/26
最近更新日期
2023/07/12
药物ATC编码
J01XX08 linezolid
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_impack_clean
Date of last change:2024/09/06
Final Product Information
|
common_pl_clean
Date of last change:2024/09/06
Final Product Information
|
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