欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/1794/001
药品名称
Ultracortenol
活性成分
Prednisolone pivalate 5.0 mg/g
剂型
Eye ointment
上市许可持有人
Agepha Pharma s.r.o., Slovakia
参考成员国 - 产品名称
Sweden (SE)
Ultracortenol
互认成员国 - 产品名称
France (FR)
Poland (PL)
Latvia (LV)
Ultarcorlene 5 mg/g acu ziede
Lithuania (LT)
Ultarcorlene 5 mg/g akių tepalas
Estonia (EE)
ULTRACORTENOL
Romania (RO)
Slovenia (SI)
Ultracortenol 5 mg/g mazilo za oko
Malta (MT)
Croatia (HR)
Ultracortenol 5 mg/g mast za oko
许可日期
2020/10/22
最近更新日期
2025/01/23
药物ATC编码
S01BA04 prednisolone
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
PubAR
|
https___www_lakemedelsverket_se_sv_sok_lakemedelsfakta_lakemedel_id_19580930000014
Date of last change:2024/09/06
PubAR Summary
|
https___www_lakemedelsverket_se_sv_sok_lakemedelsfakta_lakemedel_id_19580930000014_2
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase