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
71335-2447-2	71335-2447	HUMAN PRESCRIPTION DRUG	Potassium Chloride Extended-Release	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20240918	N/A	ANDA	ANDA209688	Bryant Ranch Prepack	POTASSIUM CHLORIDE	750 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-2)
71335-2447-3	71335-2447	HUMAN PRESCRIPTION DRUG	Potassium Chloride Extended-Release	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20240918	N/A	ANDA	ANDA209688	Bryant Ranch Prepack	POTASSIUM CHLORIDE	750 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-3)
71335-2447-4	71335-2447	HUMAN PRESCRIPTION DRUG	Potassium Chloride Extended-Release	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20240918	N/A	ANDA	ANDA209688	Bryant Ranch Prepack	POTASSIUM CHLORIDE	750 mg/1	15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-4)
71335-2447-5	71335-2447	HUMAN PRESCRIPTION DRUG	Potassium Chloride Extended-Release	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20240918	N/A	ANDA	ANDA209688	Bryant Ranch Prepack	POTASSIUM CHLORIDE	750 mg/1	180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-5)
71335-2447-6	71335-2447	HUMAN PRESCRIPTION DRUG	Potassium Chloride Extended-Release	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20240918	N/A	ANDA	ANDA209688	Bryant Ranch Prepack	POTASSIUM CHLORIDE	750 mg/1	28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-6)
71335-2447-7	71335-2447	HUMAN PRESCRIPTION DRUG	Potassium Chloride Extended-Release	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20240918	N/A	ANDA	ANDA209688	Bryant Ranch Prepack	POTASSIUM CHLORIDE	750 mg/1	10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-7)