欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
FR/H/0149/001
药品名称
Pulmotec
活性成分
high purity graphite 99.9 %
剂型
[not specified]
上市许可持有人
MDS Nordion SA
参考成员国 - 产品名称
France (FR)
互认成员国 - 产品名称
Hungary (HU)
Denmark (DK)
Croatia (HR)
Iceland (IS)
Sweden (SE)
Greece (EL)
Italy (IT)
Portugal (PT)
Spain (ES)
Austria (AT)
Pulmotec Graphittiegel zur Bereitung von Technegas zur Inhalation
Ireland (IE)
United Kingdom (Northern Ireland) (XI)
Luxembourg (LU)
Netherlands (NL)
Belgium (BE)
Germany (DE)
Slovenia (SI)
Slovak Republic (SK)
Pulmotec, graphite crucible for the preparation of Technegas inhalation
Czech Republic (CZ)
Pulmotec, graphite crucible for the preparation of Technegas inhalation
Finland (FI)
Poland (PL)
Norway (NO)
许可日期
1999/12/01
最近更新日期
2025/09/08
药物ATC编码
V04D DIAGNOSTIC RADIOPHARMACEUTICALS
申请类型
TypeLevel1:
TypeLevel2:
TypeLevel3:
TypeLevel4:
TypeLevel5:
附件文件下载
Final Product Information
|
Pulmotec_common_PI_v028_cl
Date of last change:2025/09/08
Final SPC
|
common_combined_cl
Date of last change:2024/12/19
市场状态
Positive
©2006-2026
Drugfuture
->
European Union HMA Authorisation of Medicines DataBase