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
60760-293-90	60760-293	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200916	N/A	NDA AUTHORIZED GENERIC	NDA018279	St. Mary's Medical Park Pharmacy	POTASSIUM CHLORIDE	750 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-293-90)
71335-1050-1	71335-1050	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20131212	N/A	NDA AUTHORIZED GENERIC	NDA018279	Bryant Ranch Prepack	POTASSIUM CHLORIDE	750 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1050-1)
71335-1050-2	71335-1050	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20131212	N/A	NDA AUTHORIZED GENERIC	NDA018279	Bryant Ranch Prepack	POTASSIUM CHLORIDE	750 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1050-2)
71335-1050-3	71335-1050	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20131212	N/A	NDA AUTHORIZED GENERIC	NDA018279	Bryant Ranch Prepack	POTASSIUM CHLORIDE	750 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1050-3)
71335-1050-4	71335-1050	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20131212	N/A	NDA AUTHORIZED GENERIC	NDA018279	Bryant Ranch Prepack	POTASSIUM CHLORIDE	750 mg/1	15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1050-4)
71335-1050-5	71335-1050	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20131212	N/A	NDA AUTHORIZED GENERIC	NDA018279	Bryant Ranch Prepack	POTASSIUM CHLORIDE	750 mg/1	180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1050-5)
71335-1050-6	71335-1050	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20131212	N/A	NDA AUTHORIZED GENERIC	NDA018279	Bryant Ranch Prepack	POTASSIUM CHLORIDE	750 mg/1	28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1050-6)
71335-1050-7	71335-1050	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190111	N/A	NDA AUTHORIZED GENERIC	NDA018279	Bryant Ranch Prepack	POTASSIUM CHLORIDE	750 mg/1	10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1050-7)
71335-1210-1	71335-1210	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190509	N/A	NDA AUTHORIZED GENERIC	NDA018279	Bryant Ranch Prepack	POTASSIUM CHLORIDE	750 mg/1	180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1210-1)
66267-259-90	66267-259	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20161107	N/A	NDA AUTHORIZED GENERIC	NDA018279	NuCare Pharmaceuticals, Inc.	POTASSIUM CHLORIDE	750 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (66267-259-90)
66267-259-30	66267-259	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20161107	N/A	NDA AUTHORIZED GENERIC	NDA018279	NuCare Pharmaceuticals, Inc.	POTASSIUM CHLORIDE	750 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (66267-259-30)
71335-1315-1	71335-1315	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190827	N/A	NDA AUTHORIZED GENERIC	NDA018279	Bryant Ranch Prepack	POTASSIUM CHLORIDE	750 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1315-1)
71335-1315-5	71335-1315	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190827	N/A	NDA AUTHORIZED GENERIC	NDA018279	Bryant Ranch Prepack	POTASSIUM CHLORIDE	750 mg/1	180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1315-5)
71335-1315-6	71335-1315	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190827	N/A	NDA AUTHORIZED GENERIC	NDA018279	Bryant Ranch Prepack	POTASSIUM CHLORIDE	750 mg/1	28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1315-6)
71335-1315-7	71335-1315	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190827	N/A	NDA AUTHORIZED GENERIC	NDA018279	Bryant Ranch Prepack	POTASSIUM CHLORIDE	750 mg/1	10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1315-7)
71335-1315-2	71335-1315	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190827	N/A	NDA AUTHORIZED GENERIC	NDA018279	Bryant Ranch Prepack	POTASSIUM CHLORIDE	750 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1315-2)
71335-1315-3	71335-1315	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190827	N/A	NDA AUTHORIZED GENERIC	NDA018279	Bryant Ranch Prepack	POTASSIUM CHLORIDE	750 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1315-3)
71335-1315-4	71335-1315	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190827	N/A	NDA AUTHORIZED GENERIC	NDA018279	Bryant Ranch Prepack	POTASSIUM CHLORIDE	750 mg/1	15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1315-4)
68382-320-01	68382-320	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170601	N/A	NDA AUTHORIZED GENERIC	NDA018279	Zydus Pharmaceuticals USA Inc	POTASSIUM CHLORIDE	750 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-320-01)
68382-320-10	68382-320	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170601	N/A	NDA AUTHORIZED GENERIC	NDA018279	Zydus Pharmaceuticals USA Inc	POTASSIUM CHLORIDE	750 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-320-10)