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

MR编号	AT/H/0121/002
药品名称	Biodroxil 1000 mg -Filmtabletten
活性成分	cefadroxil monohydrate 0.0 mg
剂型	Film-coated tablet
上市许可持有人	Sandoz GmbH Biochemiestraße 10 A-6250 Kundl
参考成员国 - 产品名称	Austria (AT) Biodroxil 1000 mg - Filmtabletten
互认成员国 - 产品名称
许可日期	2002/06/11
最近更新日期	2022/05/10
药物ATC编码	J01DA09 Cefadroxil
申请类型	TypeLevel1：Abridged TypeLevel2：Additional Strength/Form TypeLevel3：Generic Article 4.8(a)(iii), first paragraph TypeLevel4：Chemical Substance TypeLevel5：Prescription Only
附件文件下载	Final SPC \| final_spc_AT_H_0121_003_IB_037_biodroxil_250mg5ml_cleanDate of last change:2019/09/06 Final SPC \| final_spc_AT_H_0121_001_IB_037_biodroxil_500mg_cleanDate of last change:2019/09/06 Final SPC \| final_spc_AT_H_0121_002_IB_037_1000mg_cleanDate of last change:2019/09/06 Final PL \| final_pl_AT_H_0121_002_IB_037_1000mg_cleanDate of last change:2019/09/06 Final SPC \| final_spc_AT_H_0121_004_IB_037_biodroxil_500mg5ml_cleanDate of last change:2019/09/06 Final PL \| final_pl_AT_H_0121_001_IB_037_biodroxil_500mg_cleanDate of last change:2019/09/06 Final Labelling \| final_lab_AT_H_0121_003_IB_037_biodroxil_250mg5ml_cleanDate of last change:2019/09/06 Final PL \| final_pl_AT_H_0121_003_IB_037_250mg5ml_cleanDate of last change:2019/09/06 Final PL \| final_pl_AT_H_0121_004_IB_037_500mg5ml_cleanDate of last change:2019/09/06 Final Labelling \| final_lab_AT_H_0121_004_IB_037_biodroxil_500mg5ml_cleanDate of last change:2019/09/06 PAR \| AT_H_0121_001-004_PAR_BiodroxilDate of last change:2016/09/13
市场状态	Positive