欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）

MR编号	SK/H/0148/001
药品名称	Azithromycin Krka 250 mg filmom obalené tablety
活性成分	azithromycin dihydrate 250.0 mg
剂型	Film-coated tablet
上市许可持有人	Krka, d.d., Novo mesto Šmarješka cesta 6 Novo Mesto 8501 Slovenia
参考成员国 - 产品名称	Slovakia (SK) Azitromycin Krka 250 mg filmom obalené tablety
互认成员国 - 产品名称	Ireland (IE) Spain (ES) Italy (IT) Sweden (SE) Finland (FI) Poland (PL) Azithromycin Krka Lithuania (LT) Azibiot 250 mg plėvele dengtos tabletės Estonia (EE) AZITHROMYCIN KRKA Bulgaria (BG) Azibiot Czechia (CZ) AZIBIOT NEO 250 MG Slovenia (SI)
许可日期	2014/03/21
最近更新日期	2024/04/08
药物ATC编码	J01FA10 azithromycin
申请类型	TypeLevel1：Known Active Substance TypeLevel2：Initial Application 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 \| common_combined_clean_plu por_SK_0148_001_004_II_020_EoP Date of last change:2022/09/05 Final Product Information \| common_combined_track_plu por_SK_0148_001_004_II_020_EoP Date of last change:2022/09/05 Final Product Information \| common_combined_track_tbl flm_SK_0148_001_004_II_020_EoP Date of last change:2022/09/05 Final Product Information \| common_combined_clean_tbl flm_SK_0148_001_004_II_020_EoP Date of last change:2022/09/05 PAR Summary \| PAR_summary_Azibiot NEODate of last change:2017/06/30 PAR \| PAR_Azibiot NEODate of last change:2017/06/30 Final SPC \| Azithromycn Krka 250 mg SK_H_0148_001_IB_003Date of last change:2015/07/09
市场状态	Positive