欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/0129/001
药品名称
Propess
活性成分
dinoprostone 10.0 mg
剂型
Vaginal device
上市许可持有人
Ferring Läkemedel AB Sverige
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Ireland (IE)
Finland (FI)
Latvia (LV)
Propess 10 mg vaginālās ievadīšanas sistēma
Norway (NO)
Poland (PL)
Cervidil
Bulgaria (BG)
Propess
Cyprus (CY)
PROPESS 10mg vaginal delivery system
Estonia (EE)
Czechia (CZ)
Propess
Lithuania (LT)
-
Romania (RO)
PROPESS 10 mg/24 ore sistem cu cedare vaginală
Slovakia (SK)
Croatia (HR)
Slovenia (SI)
Germany (DE)
Propess 10 mg Vaginalinsert
Denmark (DK)
Belgium (BE)
Netherlands (NL)
Luxembourg (LU)
Propess
United Kingdom (Northern Ireland) (XI)
Propess
Austria (AT)
Propess 10 mg vaginales Freisetzungssystem
Spain (ES)
Portugal (PT)
Italy (IT)
Greece (GR)
许可日期
1997/10/02
最近更新日期
2024/07/02
药物ATC编码
G02AD02 dinoprostone
申请类型
TypeLevel1:
[not specified]
TypeLevel2:
[not specified]
TypeLevel3:
[not specified]
TypeLevel4:
[not specified]
TypeLevel5:
[not specified]
附件文件下载
Final PL
|
SE_H_0129_001_Final PL
Date of last change:2024/09/06
Final SPC
|
SE_H_0129_001_Final SPC
Date of last change:2024/09/06
PubAR
|
SE_H_0129_001_PAR
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase