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
24979-229-01	24979-229	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20241028	N/A	ANDA	ANDA218979	Upsher-Smith Laboratories, LLC	POTASSIUM CHLORIDE	600 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-229-01)
24979-229-02	24979-229	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20241028	N/A	ANDA	ANDA218979	Upsher-Smith Laboratories, LLC	POTASSIUM CHLORIDE	600 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-229-02)
24979-230-02	24979-230	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20241028	N/A	ANDA	ANDA218979	Upsher-Smith Laboratories, LLC	POTASSIUM CHLORIDE	750 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-230-02)
24979-230-01	24979-230	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20241028	N/A	ANDA	ANDA218979	Upsher-Smith Laboratories, LLC	POTASSIUM CHLORIDE	750 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-230-01)