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
16571-842-01	16571-842	HUMAN PRESCRIPTION DRUG	POTASSIUM CHLORIDE EXTENDED RELEASE	potassium chloride	TABLET, EXTENDED RELEASE	ORAL	20250213	N/A	ANDA	ANDA217412	Rising Pharma Holdings, Inc.	POTASSIUM CHLORIDE	600 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-842-01)
16571-842-50	16571-842	HUMAN PRESCRIPTION DRUG	POTASSIUM CHLORIDE EXTENDED RELEASE	potassium chloride	TABLET, EXTENDED RELEASE	ORAL	20250213	N/A	ANDA	ANDA217412	Rising Pharma Holdings, Inc.	POTASSIUM CHLORIDE	600 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-842-50)
16571-843-01	16571-843	HUMAN PRESCRIPTION DRUG	POTASSIUM CHLORIDE EXTENDED RELEASE	potassium chloride	TABLET, EXTENDED RELEASE	ORAL	20250213	N/A	ANDA	ANDA217412	Rising Pharma Holdings, Inc.	POTASSIUM CHLORIDE	750 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-843-01)
16571-843-50	16571-843	HUMAN PRESCRIPTION DRUG	POTASSIUM CHLORIDE EXTENDED RELEASE	potassium chloride	TABLET, EXTENDED RELEASE	ORAL	20250213	N/A	ANDA	ANDA217412	Rising Pharma Holdings, Inc.	POTASSIUM CHLORIDE	750 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-843-50)