美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=POTASSIUM CHLORIDE"
符合检索条件的记录共293
30 页 当前第 1 页  下一页 最后一页 返回检索页
1药品名称POTASSIUM CHLORIDE
申请号007865产品号002
活性成分POTASSIUM CHLORIDE市场状态停止上市
剂型或给药途径INJECTABLE;INJECTION规格2MEQ/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ELI LILLY AND CO
2药品名称DEXTROSE 5% AND POTASSIUM CHLORIDE 0.15% IN PLASTIC CONTAINER
申请号017634产品号001
活性成分DEXTROSE; POTASSIUM CHLORIDE市场状态处方药
剂型或给药途径INJECTABLE;INJECTION规格5GM/100ML;150MG/100ML
治疗等效代码AP参比药物
批准日期Approved Prior to Jan 1, 1982申请机构BAXTER HEALTHCARE CORP
3药品名称DEXTROSE 5% AND POTASSIUM CHLORIDE 0.3% IN PLASTIC CONTAINER
申请号017634产品号002
活性成分DEXTROSE; POTASSIUM CHLORIDE市场状态处方药
剂型或给药途径INJECTABLE;INJECTION规格5GM/100ML;300MG/100ML
治疗等效代码AP参比药物
批准日期Approved Prior to Jan 1, 1982申请机构BAXTER HEALTHCARE CORP
4药品名称DEXTROSE 5% AND POTASSIUM CHLORIDE 0.224% IN PLASTIC CONTAINER
申请号017634产品号003
活性成分DEXTROSE; POTASSIUM CHLORIDE市场状态处方药
剂型或给药途径INJECTABLE;INJECTION规格5GM/100ML;224MG/100ML
治疗等效代码AP参比药物
批准日期Approved Prior to Jan 1, 1982申请机构BAXTER HEALTHCARE CORP
5药品名称DEXTROSE 5% AND POTASSIUM CHLORIDE 0.075% IN PLASTIC CONTAINER
申请号017634产品号004
活性成分DEXTROSE; POTASSIUM CHLORIDE市场状态处方药
剂型或给药途径INJECTABLE;INJECTION规格5GM/100ML;75MG/100ML
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构BAXTER HEALTHCARE CORP
6药品名称POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
申请号017648产品号001
活性成分POTASSIUM CHLORIDE; SODIUM CHLORIDE市场状态处方药
剂型或给药途径INJECTABLE;INJECTION规格150MG/100ML;900MG/100ML
治疗等效代码AP参比药物
批准日期Approved Prior to Jan 1, 1982申请机构BAXTER HEALTHCARE CORP
7药品名称POTASSIUM CHLORIDE 0.3% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
申请号017648产品号002
活性成分POTASSIUM CHLORIDE; SODIUM CHLORIDE市场状态处方药
剂型或给药途径INJECTABLE;INJECTION规格300MG/100ML;900MG/100ML
治疗等效代码AP参比药物
批准日期Approved Prior to Jan 1, 1982申请机构BAXTER HEALTHCARE CORP
8药品名称POTASSIUM CHLORIDE 0.224% IN SODIUM CHLORIDE 0.9%
申请号017648产品号003
活性成分POTASSIUM CHLORIDE; SODIUM CHLORIDE市场状态处方药
剂型或给药途径INJECTABLE;INJECTION规格224MG/100ML;900MG/100ML
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构BAXTER HEALTHCARE CORP
9药品名称SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.075% IN PLASTIC CONTAINER
申请号017648产品号004
活性成分POTASSIUM CHLORIDE; SODIUM CHLORIDE市场状态停止上市
剂型或给药途径INJECTABLE;INJECTION规格75MG/100ML;900MG/100ML
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构BAXTER HEALTHCARE CORP
10药品名称POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER
申请号017648产品号005
活性成分POTASSIUM CHLORIDE; SODIUM CHLORIDE市场状态处方药
剂型或给药途径INJECTABLE;INJECTION规格150MG/100ML;450MG/100ML
治疗等效代码AP参比药物
批准日期2002/11/26申请机构BAXTER HEALTHCARE CORP