欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/2430/002
药品名称
Vellena
活性成分
ethinyl estradiol 30.0 µg
gestodene 75.0 µg
剂型
Coated tablet
上市许可持有人
Actavis Group PTC ehf Reykjavikurvegur 76-78 220 IS Hafnarfjordur Iceland
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Denmark (DK)
Vellena
许可日期
2008/08/13
最近更新日期
2024/01/31
药物ATC编码
G03AA10 gestodene and ethinylestradiol
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 Labelling
|
DK_H_1148_001_002_IB_011_Vellena_Final_LAB_CL
Date of last change:2024/09/06
Final PL
|
DK_H_1148_001_002_IB_011_Vellena_Final_PL_CL
Date of last change:2024/09/06
Final SPC
|
DK_H_1148_001_002_IB_011_Vellena_Final_SmPC_CL
Date of last change:2024/09/06
PubAR
|
parmod5_dk1148vellena_pdf
Date of last change:2024/09/06
Final Product Information
|
PIL_clean
Date of last change:2024/09/06
Final Product Information
|
SmPC_clean
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase