美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件: 药品名称=ERYTHROMYCIN ETHYLSUCCINATE
符合检索条件的记录共14
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1药品名称ERYTHROMYCIN ETHYLSUCCINATE
申请号061904产品号001
活性成分ERYTHROMYCIN ETHYLSUCCINATE市场状态处方药
剂型或给药途径TABLET;ORAL规格EQ 400MG BASE
治疗等效代码BX参比药物
批准日期Approved Prior to Jan 1, 1982申请机构ARBOR PHARMACEUTICALS LLC
2药品名称ERYTHROMYCIN ETHYLSUCCINATE
申请号062055产品号001
活性成分ERYTHROMYCIN ETHYLSUCCINATE市场状态停止上市
剂型或给药途径GRANULE;ORAL规格EQ 200MG BASE/5ML
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构ANI PHARMACEUTICALS INC
3药品名称ERYTHROMYCIN ETHYLSUCCINATE
申请号062177产品号001
活性成分ERYTHROMYCIN ETHYLSUCCINATE市场状态停止上市
剂型或给药途径SUSPENSION;ORAL规格EQ 200MG BASE/5ML
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构DISTA PRODUCTS CO DIV ELI LILLY AND CO
4药品名称ERYTHROMYCIN ETHYLSUCCINATE
申请号062177产品号002
活性成分ERYTHROMYCIN ETHYLSUCCINATE市场状态停止上市
剂型或给药途径SUSPENSION;ORAL规格EQ 400MG BASE/5ML
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构DISTA PRODUCTS CO DIV ELI LILLY AND CO
5药品名称ERYTHROMYCIN ETHYLSUCCINATE
申请号062200产品号001
活性成分ERYTHROMYCIN ETHYLSUCCINATE市场状态停止上市
剂型或给药途径SUSPENSION;ORAL规格EQ 200MG BASE/5ML
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构ALPHARMA US PHARMACEUTICALS DIVISION
6药品名称ERYTHROMYCIN ETHYLSUCCINATE
申请号062200产品号002
活性成分ERYTHROMYCIN ETHYLSUCCINATE市场状态停止上市
剂型或给药途径SUSPENSION;ORAL规格EQ 400MG BASE/5ML
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构ALPHARMA US PHARMACEUTICALS DIVISION
7药品名称ERYTHROMYCIN ETHYLSUCCINATE
申请号062231产品号001
活性成分ERYTHROMYCIN ETHYLSUCCINATE市场状态停止上市
剂型或给药途径SUSPENSION;ORAL规格EQ 200MG BASE/5ML
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构PARKE DAVIS DIV WARNER LAMBERT CO
8药品名称ERYTHROMYCIN ETHYLSUCCINATE
申请号062231产品号002
活性成分ERYTHROMYCIN ETHYLSUCCINATE市场状态停止上市
剂型或给药途径SUSPENSION;ORAL规格EQ 400MG BASE/5ML
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构PARKE DAVIS DIV WARNER LAMBERT CO
9药品名称ERYTHROMYCIN ETHYLSUCCINATE
申请号062256产品号001
活性成分ERYTHROMYCIN ETHYLSUCCINATE市场状态停止上市
剂型或给药途径TABLET;ORAL规格EQ 400MG BASE
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构BARR LABORATORIES INC
10药品名称ERYTHROMYCIN ETHYLSUCCINATE
申请号062558产品号001
活性成分ERYTHROMYCIN ETHYLSUCCINATE市场状态停止上市
剂型或给药途径SUSPENSION;ORAL规格EQ 400MG BASE/5ML
治疗等效代码参比药物
批准日期1985/03/15申请机构PHARMAFAIR INC