欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
FR/V/0282/001
药品名称
NEOMAY 500 mg/g
活性成分
neomycin 50.0 %
剂型
Powder for oral solution
上市许可持有人
Laboratorios Maymó
参考成员国 - 产品名称
France (FR)
13830
互认成员国 - 产品名称
Denmark (DK)
Spain (ES)
Portugal (PT)
Italy (IT)
United Kingdom (Northern Ireland) (XI)
Ireland (IE)
Neomay 500 IU/g Powder for use in drinking water/milk
Greece (GR)
Hungary (HU)
Poland (PL)
Czechia (CZ)
NEOMAY 500 000 IU/g prášek pro podání v pitné vodě/mléčné náhražce
Romania (RO)
Slovenia (SI)
Slovakia (SK)
Croatia (HR)
许可日期
2015/09/23
最近更新日期
2022/11/23
药物ATC编码
QA07AA01 neomycin
申请类型
TypeLevel1:
[not specified]
TypeLevel2:
[not specified]
TypeLevel3:
Other Generic application Art 13.3 Dir 2001/82/EC
TypeLevel4:
[not specified]
TypeLevel5:
[not specified]
附件文件下载
Final SPC
|
13830 D90 SPC
Date of last change:2024/09/06
Final PL
|
1b1_pl_neomay_rup_d89_commit_track
Date of last change:2024/09/06
Final Labelling
|
1b1_pl_neomay_varIB_280218
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase