欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
FR/H/0282/003
药品名称
Fostimon 150 IU/mL
活性成分
urofollitropin 75.0 IU
剂型
Solution for injection
上市许可持有人
Genevrier Parc Sofia Antipolis France
参考成员国 - 产品名称
France (FR)
互认成员国 - 产品名称
Denmark (DK)
Belgium (BE)
Netherlands (NL)
Luxembourg (LU)
United Kingdom (Northern Ireland) (XI)
Ireland (IE)
Austria (AT)
Fostimon 150 IU/1 ml - Pulver und Lösungsmittel zur Herstellung einer Injektionslösung
Spain (ES)
Sweden (SE)
Fostimon Set
Norway (NO)
Finland (FI)
Cyprus (CY)
FOSTIMON PWD AND SOLVENT IN PFS
许可日期
2011/10/27
最近更新日期
2024/03/07
药物ATC编码
G GENITO URINARY SYSTEM AND SEX HORMONES
申请类型
TypeLevel1:
Known Active Substance
TypeLevel2:
Additional Strength/Form
TypeLevel3:
Full Dossier Art 8.3(i) Dir 2001/83/EC
TypeLevel4:
Biological: Other
TypeLevel5:
Prescription Only
附件文件下载
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase