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
72865-195-05	72865-195	HUMAN PRESCRIPTION DRUG	POTASSIUM CHLORIDE	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20210304	N/A	ANDA	ANDA214422	XLCare Pharmaceuticals, Inc.	POTASSIUM CHLORIDE	1125 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-195-05)
31722-135-05	31722-135	HUMAN PRESCRIPTION DRUG	POTASSIUM CHLORIDE	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20210120	N/A	ANDA	ANDA214422	Camber Pharmaceuticals, Inc.	POTASSIUM CHLORIDE	1500 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-135-05)
72865-194-01	72865-194	HUMAN PRESCRIPTION DRUG	POTASSIUM CHLORIDE	Potassium CHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20210304	N/A	ANDA	ANDA214422	XLCare Pharmaceuticals, Inc.	POTASSIUM CHLORIDE	750 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-194-01)
72865-194-05	72865-194	HUMAN PRESCRIPTION DRUG	POTASSIUM CHLORIDE	Potassium CHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20210304	N/A	ANDA	ANDA214422	XLCare Pharmaceuticals, Inc.	POTASSIUM CHLORIDE	750 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-194-05)
72603-337-01	72603-337	HUMAN PRESCRIPTION DRUG	potassium chloride	potassium chloride	TABLET, EXTENDED RELEASE	ORAL	20240621	N/A	ANDA	ANDA214422	Northstar Rx LLC	POTASSIUM CHLORIDE	750 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72603-337-01)
72865-196-01	72865-196	HUMAN PRESCRIPTION DRUG	POTASSIUM CHLORIDE	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20210304	N/A	ANDA	ANDA214422	XLCare Pharmaceuticals, Inc.	POTASSIUM CHLORIDE	1500 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-196-01)
72865-196-05	72865-196	HUMAN PRESCRIPTION DRUG	POTASSIUM CHLORIDE	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20210304	N/A	ANDA	ANDA214422	XLCare Pharmaceuticals, Inc.	POTASSIUM CHLORIDE	1500 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-196-05)
31722-133-01	31722-133	HUMAN PRESCRIPTION DRUG	POTASSIUM CHLORIDE	Potassium CHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20210120	N/A	ANDA	ANDA214422	Camber Pharmaceuticals, Inc.	POTASSIUM CHLORIDE	750 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-133-01)
31722-133-05	31722-133	HUMAN PRESCRIPTION DRUG	POTASSIUM CHLORIDE	Potassium CHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20210120	N/A	ANDA	ANDA214422	Camber Pharmaceuticals, Inc.	POTASSIUM CHLORIDE	750 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-133-05)
43602-284-05	43602-284	HUMAN PRESCRIPTION DRUG	POTASSIUM CHLORIDE	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20201230	N/A	ANDA	ANDA214422	Ascent Pharmaceuticals, Inc.	POTASSIUM CHLORIDE	1125 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (43602-284-05)
43602-284-30	43602-284	HUMAN PRESCRIPTION DRUG	POTASSIUM CHLORIDE	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20201230	N/A	ANDA	ANDA214422	Ascent Pharmaceuticals, Inc.	POTASSIUM CHLORIDE	1125 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (43602-284-30)
72603-338-01	72603-338	HUMAN PRESCRIPTION DRUG	potassium chloride	potassium chloride	TABLET, EXTENDED RELEASE	ORAL	20190621	N/A	ANDA	ANDA214422	Northstar Rx LLC	POTASSIUM CHLORIDE	1500 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72603-338-01)
31722-134-01	31722-134	HUMAN PRESCRIPTION DRUG	POTASSIUM CHLORIDE	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20210120	N/A	ANDA	ANDA214422	Camber Pharmaceuticals, Inc.	POTASSIUM CHLORIDE	1125 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-134-01)
43602-285-05	43602-285	HUMAN PRESCRIPTION DRUG	POTASSIUM CHLORIDE	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20201230	N/A	ANDA	ANDA214422	Ascent Pharmaceuticals, Inc.	POTASSIUM CHLORIDE	1500 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (43602-285-05)
43602-285-30	43602-285	HUMAN PRESCRIPTION DRUG	POTASSIUM CHLORIDE	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20201230	N/A	ANDA	ANDA214422	Ascent Pharmaceuticals, Inc.	POTASSIUM CHLORIDE	1500 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (43602-285-30)