欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/1550/003
药品名称
Jimandin
活性成分
SITAGLIPTIN 100.0 mg
剂型
Film-coated tablet
上市许可持有人
Medochemie Ltd. Cyprus
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Greece (GR)
JIMANDIN
Latvia (LV)
Jimandin 100 mg apvalkotās tabletes
Lithuania (LT)
JIMANDIN 100 mg plėvele dengtos tabletės
Estonia (EE)
JIMANDIN
Bulgaria (BG)
Jimandin
Cyprus (CY)
Czechia (CZ)
JIMANDIN
Romania (RO)
JIMANDIN 100 mg comprimate filmate
Slovakia (SK)
JIMANDIN 100 mg filmom obalené tablety
Malta (MT)
Jimandin 100 mg film-coated tablets
Croatia (HR)
Jimandin 100 mg filmom obložene tablete
许可日期
2017/06/21
最近更新日期
2021/12/02
药物ATC编码
A10BH01 sitagliptin
申请类型
TypeLevel1:
Known Active Substance
TypeLevel2:
Additional Strength/Form
TypeLevel3:
Generic Art 10.1 and 10.2 Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final PL
|
SE_H_1550_003_Final PL
Date of last change:2024/09/06
Final SPC
|
SE_H_1550_003_Final SPC
Date of last change:2024/09/06
PubAR
|
SE_H_1550_003_PAR
Date of last change:2024/09/06
PubAR Summary
|
SE_H_1550_003_PAR Summary
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase