美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=RINGER'S IN PLASTIC CONTAINER"
符合检索条件的记录共47
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41药品名称POTASSIUM CHLORIDE 10MEQ IN DEXTROSE 5% AND LACTATED RINGER'S IN PLASTIC CONTAINER
申请号019685产品号005
活性成分CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE市场状态停止上市
剂型或给药途径INJECTABLE;INJECTION规格20MG/100ML;5GM/100ML;104MG/100ML;600MG/100ML;310MG/100ML
治疗等效代码参比药物
批准日期1988/10/17申请机构HOSPIRA INC
42药品名称POTASSIUM CHLORIDE 10MEQ IN DEXTROSE 5% AND LACTATED RINGER'S IN PLASTIC CONTAINER
申请号019685产品号006
活性成分CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE市场状态停止上市
剂型或给药途径INJECTABLE;INJECTION规格20MG/100ML;5GM/100ML;179MG/100ML;600MG/100ML;310MG/100ML
治疗等效代码参比药物
批准日期1988/10/17申请机构HOSPIRA INC
43药品名称POTASSIUM CHLORIDE 15MEQ IN DEXTROSE 5% AND LACTATED RINGER'S IN PLASTIC CONTAINER
申请号019685产品号007
活性成分CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE市场状态停止上市
剂型或给药途径INJECTABLE;INJECTION规格20MG/100ML;5GM/100ML;254MG/100ML;600MG/100ML;310MG/100ML
治疗等效代码参比药物
批准日期1988/10/17申请机构HOSPIRA INC
44药品名称POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% AND LACTATED RINGER'S IN PLASTIC CONTAINER
申请号019685产品号008
活性成分CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE市场状态处方药
剂型或给药途径INJECTABLE;INJECTION规格20MG/100ML;5GM/100ML;328MG/100ML;600MG/100ML;310MG/100ML
治疗等效代码AP参比药物
批准日期1988/10/17申请机构HOSPIRA INC
45药品名称LACTATED RINGER'S IN PLASTIC CONTAINER
申请号019933产品号001
活性成分CALCIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE市场状态停止上市
剂型或给药途径SOLUTION;IRRIGATION规格20MG/100ML;30MG/100ML;600MG/100ML;310MG/100ML
治疗等效代码参比药物
批准日期1989/08/29申请机构BAXTER HEALTHCARE CORP
46药品名称DEXTROSE 5% IN RINGER'S IN PLASTIC CONTAINER
申请号020000产品号001
活性成分CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE市场状态处方药
剂型或给药途径INJECTABLE;INJECTION规格33MG/100ML;5GM/100ML;30MG/100ML;860MG/100ML
治疗等效代码AP参比药物
批准日期1992/04/17申请机构B BRAUN MEDICAL INC
47药品名称RINGER'S IN PLASTIC CONTAINER
申请号020002产品号001
活性成分CALCIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE市场状态处方药
剂型或给药途径INJECTABLE;INJECTION规格33MG/100ML;30MG/100ML;860MG/100ML
治疗等效代码AP参比药物
批准日期1992/04/17申请机构B BRAUN MEDICAL INC