美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=DIPHEN"
符合检索条件的记录共118
12 页 当前第 10 页  首页 上一页 下一页 最后一页 返回检索页
91药品名称DIPHENHYDRAMINE HYDROCHLORIDE
申请号086937产品号001
活性成分DIPHENHYDRAMINE HYDROCHLORIDE市场状态停止上市
剂型或给药途径ELIXIR;ORAL规格12.5MG/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LEDERLE LABORATORIES DIV AMERICAN CYANAMID CO
92药品名称DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE
申请号086950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LEDERLE LABORATORIES DIV AMERICAN CYANAMID CO
93药品名称DIPHENHYDRAMINE HYDROCHLORIDE
申请号087066产品号001
活性成分DIPHENHYDRAMINE HYDROCHLORIDE市场状态停止上市
剂型或给药途径INJECTABLE;INJECTION规格10MG/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LYPHOMED DIV FUJISAWA USA INC
94药品名称DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE
申请号087131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PARKE DAVIS DIV WARNER LAMBERT CO
95药品名称DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE
申请号087195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1982/02/16申请机构VALEANT PHARMACEUTICALS INTERNATIONAL
96药品名称DIPHENHYDRAMINE HYDROCHLORIDE
申请号087513产品号001
活性成分DIPHENHYDRAMINE HYDROCHLORIDE市场状态处方药
剂型或给药途径ELIXIR;ORAL规格12.5MG/5ML
治疗等效代码参比药物
批准日期1982/02/10申请机构PHARMACEUTICAL ASSOC INC DIV BEACH PRODUCTS
97药品名称DIPHENHYDRAMINE HYDROCHLORIDE
申请号087630产品号001
活性成分DIPHENHYDRAMINE HYDROCHLORIDE市场状态停止上市
剂型或给药途径CAPSULE;ORAL规格50MG
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构VANGARD LABORATORIES INC DIV MIDWAY MEDICAL CO
98药品名称DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE
申请号087708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SOLUTION;ORAL规格0.025MG/5ML;2.5MG/5ML
治疗等效代码AA参比药物
批准日期1982/05/03申请机构ROXANE LABORATORIES INC
99药品名称DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE
申请号087765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1982/03/15申请机构HIKMA PHARMACEUTICALS LLC
100药品名称DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE
申请号087842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1982/03/29申请机构USL PHARMA INC