美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件: 药品名称=SODIUM CHLORIDE 0.9%
符合检索条件的记录共213
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1药品名称SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
申请号016366产品号001
活性成分SODIUM CHLORIDE市场状态处方药
剂型或给药途径INJECTABLE;INJECTION规格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HOSPIRA INC
2药品名称SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
申请号016677产品号001
活性成分SODIUM CHLORIDE市场状态处方药
剂型或给药途径INJECTABLE;INJECTION规格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
3药品名称SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
申请号016677产品号004
活性成分SODIUM CHLORIDE市场状态处方药
剂型或给药途径INJECTABLE;INJECTION规格9MG/ML
治疗等效代码AP参比药物
批准日期1985/10/30申请机构BAXTER HEALTHCARE CORP
4药品名称DEXTROSE 5% IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
申请号016678产品号001
活性成分DEXTROSE; SODIUM CHLORIDE市场状态处方药
剂型或给药途径INJECTABLE;INJECTION规格5GM/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
5药品名称DEXTROSE 10% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
申请号016696产品号001
活性成分DEXTROSE; SODIUM CHLORIDE市场状态处方药
剂型或给药途径INJECTABLE;INJECTION规格10GM/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
6药品名称SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
申请号016733产品号001
活性成分SODIUM CHLORIDE市场状态处方药
剂型或给药途径SOLUTION;IRRIGATION规格900MG/100ML
治疗等效代码AT参比药物
批准日期Approved Prior to Jan 1, 1982申请机构B BRAUN MEDICAL INC
7药品名称SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
申请号017427产品号001
活性成分SODIUM CHLORIDE市场状态处方药
剂型或给药途径SOLUTION;IRRIGATION规格900MG/100ML
治疗等效代码AT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SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
申请号017464产品号001
活性成分SODIUM CHLORIDE市场状态处方药
剂型或给药途径INJECTABLE;INJECTION规格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B BRAUN MEDICAL INC
9药品名称SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
申请号017514产品号001
活性成分SODIUM CHLORIDE市场状态处方药
剂型或给药途径SOLUTION;IRRIGATION规格900MG/100ML
治疗等效代码AT参比药物
批准日期Approved Prior to Jan 1, 1982申请机构HOSPIRA INC
10药品名称DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
申请号017585产品号001
活性成分DEXTROSE; SODIUM CHLORIDE市场状态处方药
剂型或给药途径INJECTABLE;INJECTION规格5GM/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HOSPIRA INC