欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
NL/H/0380/001
药品名称
Angeliq 1/2
活性成分
drospirenone active principles 2.0 mg
estradiol active principles 1.0 mg
剂型
Film-coated tablet
上市许可持有人
Bayer B.V. 3641 RT Mijdrecht The Netherlands
参考成员国 - 产品名称
Netherlands (NL)
互认成员国 - 产品名称
Czechia (CZ)
Slovenia (SI)
Malta (MT)
Croatia (HR)
Germany (DE)
Belgium (BE)
Luxembourg (LU)
Ireland (IE)
France (FR)
Spain (ES)
Portugal (PT)
Italy (IT)
Finland (FI)
Poland (PL)
Latvia (LV)
Lithuania (LT)
Estonia (EE)
许可日期
2003/07/04
最近更新日期
2025/09/24
药物ATC编码
G03FA Progestogens and estrogens, fixed combinations
申请类型
TypeLevel1:
Known Active Substance
TypeLevel2:
Initial Application
TypeLevel3:
Fixed Combination Article 4.8b
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final PL
|
Final EU_Angeliq_PIL_REC33711 clean_Jul 2025
Date of last change:2025/09/24
Final SPC
|
Final EU_Angeliq_SmPC_REC33711 clean_Jul 2025
Date of last change:2025/09/24
Final Labelling
|
common_interpack_1 clean
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase