欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/1849/001
药品名称
Fenylefrin Aguettant
活性成分
PHENYLEPHRINE HYDROCHLORIDE 100.0 µg/ml
剂型
Solution for injection/infusion
上市许可持有人
Laboratoire Aguettant
参考成员国 - 产品名称
Sweden (SE)
Fenylefrin Aguettant
互认成员国 - 产品名称
Germany (DE)
Denmark (DK)
Phenylephrin "Aguettant"
Belgium (BE)
Netherlands (NL)
Fenylefrine Aguettant 100 microgram/ml oplossing voor injectie of infusie
Luxembourg (LU)
United Kingdom (Northern Ireland) (XI)
Ireland (IE)
Austria (AT)
Phenylephrin Aguettant 100 Mikrogramm/ml Injektions-/Infusionslösung
France (FR)
Spain (ES)
Portugal (PT)
Norway (NO)
Fenylefrin Aguettant
Finland (FI)
Poland (PL)
Phenylephrine Aguettant
Romania (RO)
Fenilefrină Aguettant 100 micrograme/ml soluţie injectabilă/ perfuzabilă
许可日期
2019/12/19
最近更新日期
2024/06/10
药物ATC编码
C01CA06 phenylephrine
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
PAR Summary
|
Fenylefrin%20Aguettant%20100%20mikrogram%20per%20ml,%20Solution%20for%20injection%20or%20infusion%20ENG%20sPAR_09001bee8139d5ae.pdf
Date of last change:2022/05/14
PAR
|
Fenylefrin%20Aguettant%20100%20mikrogram%20per%20ml,%20Solution%20for%20injection%20or%20infusion%20ENG%20PAR_09001bee8139d5ad.pdf
Date of last change:2022/05/14
Final PL
|
SE/H/1849/001_Final PL
Date of last change:2020/02/20
Final SPC
|
SE/H/1849/001_Final SPC
Date of last change:2020/02/20
市场状态
Positive
©2006-2024
Drugfuture
->
European Union HMA Authorisation of Medicines DataBase