欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
FI/H/0665/001
药品名称
Anya
活性成分
Ethinylestradiol 20.0 µg
Levonorgestrel 90.0 µg
剂型
Film-coated tablet
上市许可持有人
Wyeth AB P.O. Box 1822 17124 Solna Sweden
参考成员国 - 产品名称
Finland (FI)
互认成员国 - 产品名称
Germany (DE)
Anya Filmtablette
Denmark (DK)
Belgium (BE)
Netherlands (NL)
Luxembourg (LU)
Iceland (IS)
United Kingdom (Northern Ireland) (XI)
Ireland (IE)
France (FR)
Portugal (PT)
Italy (IT)
Greece (GR)
Sweden (SE)
Norway (NO)
Cyprus (CY)
ANYA
许可日期
2008/09/18
最近更新日期
2024/12/12
药物ATC编码
G03AA07 levonorgestrel and ethinylestradiol
申请类型
TypeLevel1:
Known Active Substance
TypeLevel2:
Initial Application
TypeLevel3:
Full Dossier Art 8.3(i) Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
市场状态
Positive
©2006-2025
Drugfuture
->
European Union HMA Authorisation of Medicines DataBase