欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DK/H/3146/003
药品名称
Sitagliptin Mylan
活性成分
SITAGLIPTIN 100.0 mg
剂型
Film-coated tablet
上市许可持有人
Mylan AB Box 230333 10435 Stockholm Sweden
参考成员国 - 产品名称
Denmark (DK)
Sitagliptin Mylan
互认成员国 - 产品名称
Germany (DE)
Sitagliptin Mylan 100 mg Filmtabletten
Finland (FI)
Netherlands (NL)
Cyprus (CY)
Sitagliptin/Mylan 100 mg Film Coated tablets
Iceland (IS)
Sitagliptin Mylan
Czechia (CZ)
Sitagliptin Mylan
Ireland (IE)
Slovakia (SK)
Sitagliptin Mylan 100 mg
Austria (AT)
Sitagliptin Mylan 100 mg Filmtabletten
United Kingdom (Northern Ireland) (XI)
France (FR)
Spain (ES)
Portugal (PT)
Italy (IT)
Greece (GR)
Sweden (SE)
Norway (NO)
Sitagliptin Mylan
许可日期
2021/03/12
最近更新日期
2024/01/15
药物ATC编码
A10BH01 sitagliptin
申请类型
TypeLevel1:
Abridged
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 Product Information
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common_combined_clean
Date of last change:2022/06/02
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase