欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
HU/V/0140/001
药品名称
M+PAC
活性成分
mycoplasma hyopneumoniae 1.47 RPU
剂型
Emulsion for injection
上市许可持有人
INTERVET
参考成员国 - 产品名称
Hungary (HU)
互认成员国 - 产品名称
Germany (DE)
Denmark (DK)
Belgium (BE)
Luxembourg (LU)
United Kingdom (Northern Ireland) (XI)
Ireland (IE)
Austria (AT)
Spain (ES)
Portugal (PT)
Italy (IT)
Greece (GR)
Poland (PL)
Latvia (LV)
Lithuania (LT)
Estonia (EE)
Cyprus (CY)
Czechia (CZ)
Slovakia (SK)
Slovenia (SI)
Croatia (HR)
许可日期
2008/04/05
最近更新日期
2025/01/21
药物ATC编码
QI09AB13 mycoplasma
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 PL
|
WS2281_annex B_WS2281_1a_annex_eaf
Date of last change:2024/09/06
Final PL
|
WS2281_annex B_WS2281_1a_eaf
Date of last change:2024/09/06
Final SPC
|
SPC021014
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase