美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=SEPTRA"
商品名 申请号 产品号 申请类型 活性成分 剂型/给药途径 规格/剂量 RLD RS 申请号原始批准/暂定批准日期 产品号批准日期 申请人 市场状态
SEPTRA 017376 001 NDA SULFAMETHOXAZOLE; TRIMETHOPRIM TABLET;ORAL 400MG;80MG No No 1973/07/30 Approved Prior to Jan 1, 1982 MONARCH PHARMS Prescription
SEPTRA DS 017376 002 NDA SULFAMETHOXAZOLE; TRIMETHOPRIM TABLET;ORAL 800MG;160MG No No 1973/07/30 Approved Prior to Jan 1, 1982 MONARCH PHARMS Prescription
SEPTRA 017598 001 NDA SULFAMETHOXAZOLE; TRIMETHOPRIM SUSPENSION;ORAL 200MG/5ML;40MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** No No 1975/05/31 Approved Prior to Jan 1, 1982 MONARCH PHARMS Discontinued
SEPTRA GRAPE 017598 002 NDA SULFAMETHOXAZOLE; TRIMETHOPRIM SUSPENSION;ORAL 200MG/5ML;40MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** No No 1975/05/31 1986/02/12 MONARCH PHARMS Discontinued
SEPTRA 018452 001 NDA SULFAMETHOXAZOLE; TRIMETHOPRIM INJECTABLE;INJECTION 80MG/ML;16MG/ML No No 1981/06/23 Approved Prior to Jan 1, 1982 MONARCH PHARMS Discontinued
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