美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
0904-7462-62	0904-7462	HUMAN PRESCRIPTION DRUG	POTASSIUM CHLORIDE	POTASSIUM CHLORIDE	SOLUTION	ORAL	20240708	N/A	ANDA	ANDA210766	Major Pharmaceuticals	POTASSIUM CHLORIDE	40 meq/30mL	30 mL in 1 CUP, UNIT-DOSE (0904-7462-62)
0904-7462-73	0904-7462	HUMAN PRESCRIPTION DRUG	POTASSIUM CHLORIDE	POTASSIUM CHLORIDE	SOLUTION	ORAL	20240708	N/A	ANDA	ANDA210766	Major Pharmaceuticals	POTASSIUM CHLORIDE	40 meq/30mL	100 CUP, UNIT-DOSE in 1 CASE (0904-7462-73) / 30 mL in 1 CUP, UNIT-DOSE (0904-7462-62)
63739-724-50	63739-724	HUMAN PRESCRIPTION DRUG	Potassium Chloride	POTASSIUM CHLORIDE	SOLUTION	ORAL	20230825	20260731	ANDA	ANDA210766	McKesson Corporation dba SKY Packaging	POTASSIUM CHLORIDE	20 meq/15mL	5 TRAY in 1 CASE (63739-724-50) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (63739-724-01)
0121-4948-40	0121-4948	HUMAN PRESCRIPTION DRUG	Potassium Chloride	POTASSIUM CHLORIDE	SOLUTION	ORAL	20230327	N/A	ANDA	ANDA210766	PAI Holdings, LLC dba PAI Pharma	POTASSIUM CHLORIDE	20 meq/15mL	4 TRAY in 1 CASE (0121-4948-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (0121-4948-15)
0121-4948-50	0121-4948	HUMAN PRESCRIPTION DRUG	Potassium Chloride	POTASSIUM CHLORIDE	SOLUTION	ORAL	20230327	N/A	ANDA	ANDA210766	PAI Holdings, LLC dba PAI Pharma	POTASSIUM CHLORIDE	20 meq/15mL	5 TRAY in 1 CASE (0121-4948-50) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (0121-4948-15)
0121-4948-80	0121-4948	HUMAN PRESCRIPTION DRUG	Potassium Chloride	POTASSIUM CHLORIDE	SOLUTION	ORAL	20230327	N/A	ANDA	ANDA210766	PAI Holdings, LLC dba PAI Pharma	POTASSIUM CHLORIDE	20 meq/15mL	8 TRAY in 1 CASE (0121-4948-80) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (0121-4948-15)