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
67046-1261-3	67046-1261	HUMAN PRESCRIPTION DRUG	Potassium Chloride Extended-release	Potassium Chloride Extended-release	TABLET	ORAL	20241108	N/A	ANDA	ANDA214452	Coupler LLC	POTASSIUM CHLORIDE	750 mg/1	30 TABLET in 1 BLISTER PACK (67046-1261-3)
67046-1468-3	67046-1468	HUMAN PRESCRIPTION DRUG	Potassium Chloride Extended-release	Potassium Chloride Extended-release	TABLET, EXTENDED RELEASE	ORAL	20241209	N/A	ANDA	ANDA214452	Coupler LLC	POTASSIUM CHLORIDE	1500 mg/1	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-1468-3)
68001-567-00	68001-567	HUMAN PRESCRIPTION DRUG	Potassium Chloride Extended-release	Potassium Chloride Extended-release	TABLET	ORAL	20230417	N/A	ANDA	ANDA214452	Bluepoint Laboratories	POTASSIUM CHLORIDE	1500 mg/1	100 TABLET in 1 BOTTLE (68001-567-00)
68001-567-03	68001-567	HUMAN PRESCRIPTION DRUG	Potassium Chloride Extended-release	Potassium Chloride Extended-release	TABLET	ORAL	20230417	N/A	ANDA	ANDA214452	Bluepoint Laboratories	POTASSIUM CHLORIDE	1500 mg/1	500 TABLET in 1 BOTTLE (68001-567-03)
68001-566-00	68001-566	HUMAN PRESCRIPTION DRUG	Potassium Chloride Extended-release	Potassium Chloride Extended-release	TABLET	ORAL	20230417	N/A	ANDA	ANDA214452	Bluepoint Laboratories	POTASSIUM CHLORIDE	750 mg/1	100 TABLET in 1 BOTTLE (68001-566-00)
68001-566-03	68001-566	HUMAN PRESCRIPTION DRUG	Potassium Chloride Extended-release	Potassium Chloride Extended-release	TABLET	ORAL	20230417	N/A	ANDA	ANDA214452	Bluepoint Laboratories	POTASSIUM CHLORIDE	750 mg/1	500 TABLET in 1 BOTTLE (68001-566-03)
82804-109-30	82804-109	HUMAN PRESCRIPTION DRUG	Potassium Chloride Extended-release	Potassium Chloride Extended-release	TABLET, EXTENDED RELEASE	ORAL	20240614	N/A	ANDA	ANDA214452	Proficient Rx LP	POTASSIUM CHLORIDE	750 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-109-30)