欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
IT/V/0112/001
药品名称
DALMARELIN
活性成分
[No Active-Substance specified] 0.0 -
剂型
Solution for injection
上市许可持有人
Fatro S.p.A. Via Emilia, 285 Ozzano Emilia (BO) Italia
参考成员国 - 产品名称
Italy (IT)
互认成员国 - 产品名称
Belgium (BE)
Dalmarelin 25 µg/ml
Malta (MT)
Iceland (IS)
United Kingdom (Northern Ireland) (XI)
Sweden (SE)
Slovenia (SI)
Norway (NO)
Slovakia (SK)
Poland (PL)
Hungary (HU)
Germany (DE)
Dalmarelin
Netherlands (NL)
Luxembourg (LU)
Ireland (IE)
Dalmarelin 25 microgram/ml Solution for Injection
Austria (AT)
France (FR)
REPRORELINE 25 µG/ML SOLUTION INJECTABLE
Spain (ES)
Portugal (PT)
Finland (FI)
Bulgaria (BG)
Cyprus (CY)
Czechia (CZ)
Romania (RO)
Denmark (DK)
Croatia (HR)
许可日期
2003/10/29
最近更新日期
2024/04/15
药物ATC编码
A ALIMENTARY TRACT AND METABOLISM
申请类型
TypeLevel1:
[not specified]
TypeLevel2:
[not specified]
TypeLevel3:
Full Dossier (art.5)
TypeLevel4:
[not specified]
TypeLevel5:
[not specified]
附件文件下载
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase