美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE"
符合检索条件的记录共21
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1药品名称DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE
申请号040357产品号001
活性成分ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE市场状态处方药
剂型或给药途径TABLET;ORAL规格0.025MG;2.5MG
治疗等效代码AA参比药物
批准日期2000/05/02申请机构PAR PHARMACEUTICAL INC
2药品名称DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE
申请号040395产品号001
活性成分ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE市场状态停止上市
剂型或给药途径TABLET;ORAL规格0.025MG;2.5MG
治疗等效代码参比药物
批准日期2000/11/27申请机构ABLE LABORATORIES INC
3药品名称DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE
申请号085035产品号001
活性成分ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE市场状态停止上市
剂型或给药途径TABLET;ORAL规格0.025MG;2.5MG
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构R AND S PHARMA INC
4药品名称DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE
申请号085372产品号001
活性成分ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE市场状态处方药
剂型或给药途径TABLET;ORAL规格0.025MG;2.5MG
治疗等效代码AA参比药物
批准日期Approved Prior to Jan 1, 1982申请机构LANNETT CO INC
5药品名称DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE
申请号085506产品号001
活性成分ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE市场状态停止上市
剂型或给药途径TABLET;ORAL规格0.025MG;2.5MG
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构SUN PHARMACEUTICAL INDUSTRIES INC
6药品名称DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE
申请号085509产品号001
活性成分ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE市场状态停止上市
剂型或给药途径TABLET;ORAL规格0.025MG;2.5MG
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构INWOOD LABORATORIES INC SUB FOREST LABORATORIES INC
7药品名称DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE
申请号085659产品号001
活性成分ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE市场状态停止上市
剂型或给药途径TABLET;ORAL规格0.025MG;2.5MG
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构KV PHARMACEUTICAL CO
8药品名称DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE
申请号085762产品号001
活性成分ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE市场状态处方药
剂型或给药途径TABLET;ORAL规格0.025MG;2.5MG
治疗等效代码AA参比药物
批准日期Approved Prior to Jan 1, 1982申请机构MYLAN PHARMACEUTICALS INC
9药品名称DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE
申请号085766产品号001
活性成分ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE市场状态停止上市
剂型或给药途径TABLET;ORAL规格0.025MG;2.5MG
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构PRIVATE FORMULATIONS INC
10药品名称DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE
申请号085876产品号001
活性成分ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE市场状态停止上市
剂型或给药途径TABLET;ORAL规格0.025MG;2.5MG
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构WATSON LABORATORIES INC