美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件: 药品名称=SEPTRA
符合检索条件的记录共5
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1药品名称SEPTRA
申请号017376产品号001
活性成分SULFAMETHOXAZOLE; TRIMETHOPRIM市场状态处方药
剂型或给药途径TABLET;ORAL规格400MG;80MG
治疗等效代码AB参比药物
批准日期Approved Prior to Jan 1, 1982申请机构MONARCH PHARMACEUTICALS INC
2药品名称SEPTRA DS
申请号017376产品号002
活性成分SULFAMETHOXAZOLE; TRIMETHOPRIM市场状态处方药
剂型或给药途径TABLET;ORAL规格800MG;160MG
治疗等效代码AB参比药物
批准日期Approved Prior to Jan 1, 1982申请机构MONARCH PHARMACEUTICALS INC
3药品名称SEPTRA
申请号017598产品号001
活性成分SULFAMETHOXAZOLE; TRIMETHOPRIM市场状态停止上市
剂型或给药途径SUSPENSION;ORAL规格200MG/5ML;40MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构MONARCH PHARMACEUTICALS INC
4药品名称SEPTRA GRAPE
申请号017598产品号002
活性成分SULFAMETHOXAZOLE; TRIMETHOPRIM市场状态停止上市
剂型或给药途径SUSPENSION;ORAL规格200MG/5ML;40MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
治疗等效代码参比药物
批准日期1986/02/12申请机构MONARCH PHARMACEUTICALS INC
5药品名称SEPTRA
申请号018452产品号001
活性成分SULFAMETHOXAZOLE; TRIMETHOPRIM市场状态停止上市
剂型或给药途径INJECTABLE;INJECTION规格80MG/ML;16MG/ML
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构MONARCH PHARMACEUTICALS INC