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
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)
68382-398-01	68382-398	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20140116	N/A	NDA AUTHORIZED GENERIC	NDA018279	Zydus Pharmaceuticals USA Inc	POTASSIUM CHLORIDE	1500 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-398-01)
68382-600-01	68382-600	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20110222	N/A	NDA AUTHORIZED GENERIC	NDA018279	Zydus Pharmaceuticals USA Inc	POTASSIUM CHLORIDE	750 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-600-01)
68382-600-10	68382-600	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20110222	N/A	NDA AUTHORIZED GENERIC	NDA018279	Zydus Pharmaceuticals USA Inc	POTASSIUM CHLORIDE	750 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-600-10)
68382-776-01	68382-776	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20140116	N/A	NDA AUTHORIZED GENERIC	NDA018279	Zydus Pharmaceuticals USA Inc	POTASSIUM CHLORIDE	600 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-776-01)
68382-776-10	68382-776	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20140116	N/A	NDA AUTHORIZED GENERIC	NDA018279	Zydus Pharmaceuticals USA Inc	POTASSIUM CHLORIDE	600 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-776-10)
63187-610-00	63187-610	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181201	N/A	NDA AUTHORIZED GENERIC	NDA018279	Proficient Rx LP	POTASSIUM CHLORIDE	750 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-610-00)
63187-610-30	63187-610	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181201	N/A	NDA AUTHORIZED GENERIC	NDA018279	Proficient Rx LP	POTASSIUM CHLORIDE	750 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-610-30)
63187-610-60	63187-610	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181201	N/A	NDA AUTHORIZED GENERIC	NDA018279	Proficient Rx LP	POTASSIUM CHLORIDE	750 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-610-60)
63187-610-90	63187-610	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181201	N/A	NDA AUTHORIZED GENERIC	NDA018279	Proficient Rx LP	POTASSIUM CHLORIDE	750 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-610-90)