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
42806-422-01	42806-422	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230807	N/A	ANDA	ANDA209314	Epic Pharma, LLC	POTASSIUM CHLORIDE	600 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-422-01)
42806-422-05	42806-422	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230807	N/A	ANDA	ANDA209314	Epic Pharma, LLC	POTASSIUM CHLORIDE	600 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-422-05)
42806-422-10	42806-422	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230807	N/A	ANDA	ANDA209314	Epic Pharma, LLC	POTASSIUM CHLORIDE	600 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-422-10)
42806-423-01	42806-423	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230807	N/A	ANDA	ANDA209314	Epic Pharma, LLC	POTASSIUM CHLORIDE	750 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-423-01)
42806-423-05	42806-423	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230807	N/A	ANDA	ANDA209314	Epic Pharma, LLC	POTASSIUM CHLORIDE	750 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-423-05)
42806-423-10	42806-423	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230807	N/A	ANDA	ANDA209314	Epic Pharma, LLC	POTASSIUM CHLORIDE	750 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-423-10)
70436-001-01	70436-001	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181115	N/A	ANDA	ANDA209314	Slate Run Pharmaceuticals, LLC	POTASSIUM CHLORIDE	600 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70436-001-01)
70436-001-02	70436-001	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181115	N/A	ANDA	ANDA209314	Slate Run Pharmaceuticals, LLC	POTASSIUM CHLORIDE	600 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70436-001-02)
70436-001-03	70436-001	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181115	N/A	ANDA	ANDA209314	Slate Run Pharmaceuticals, LLC	POTASSIUM CHLORIDE	600 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70436-001-03)
70436-002-01	70436-002	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181115	N/A	ANDA	ANDA209314	Slate Run Pharmaceuticals, LLC	POTASSIUM CHLORIDE	750 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70436-002-01)
70436-002-02	70436-002	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181115	N/A	ANDA	ANDA209314	Slate Run Pharmaceuticals, LLC	POTASSIUM CHLORIDE	750 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70436-002-02)
70436-002-03	70436-002	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181115	N/A	ANDA	ANDA209314	Slate Run Pharmaceuticals, LLC	POTASSIUM CHLORIDE	750 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70436-002-03)
70518-3682-0	70518-3682	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230316	N/A	ANDA	ANDA209314	REMEDYREPACK INC.	POTASSIUM CHLORIDE	750 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-3682-0)