欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DK/H/3556/002
药品名称
Kosidina 0,075 mg/0,030 mg, tabletten
活性成分
ethinyl estradiol 30.0 µg
Gestodene 75.0 µg
剂型
Tablet
上市许可持有人
Sandoz B.V. Veluwezoom 22 1327 AH Almere The Netherlands
参考成员国 - 产品名称
Denmark (DK)
互认成员国 - 产品名称
许可日期
2015/11/25
最近更新日期
2025/02/06
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 Product Information
|
1_3_1 spc_label_pl _ common_outer clean 20_75_ 6_111
Date of last change:2024/09/06
Final Product Information
|
1_3_1 spc_label_pl _ common_outer clean 30_75_ 6_118
Date of last change:2024/09/06
Final Product Information
|
1_3_1 spc_label_pl _ common_pl clean 20_75_ 12_877
Date of last change:2024/09/06
Final Product Information
|
1_3_1 spc_label_pl _ common_pl clean 30_75_ 12_878
Date of last change:2024/09/06
Final Product Information
|
1_3_1 spc_label_pl _ common_spc clean 20_75_ 12_414
Date of last change:2024/09/06
Final Product Information
|
1_3_1 spc_label_pl _ common_spc clean 30_75_ 12_415
Date of last change:2024/09/06
Final Labelling
|
Common LAB 0_075_0_03_Clean version
Date of last change:2024/09/06
Final PL
|
common_pl
Date of last change:2024/09/06
Final SPC
|
common_spc
Date of last change:2024/09/06
PubAR
|
PAR_NL_H_3321_001_002_DC_Kosidina_29_9_2016
Date of last change:2024/09/06
PubAR Summary
|
summaryPAR_NL_H_3321_001_002_DC_Kosidina_29_09_2016_EN
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase