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
24979-230-00	24979-230	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20250601	N/A	ANDA	ANDA218979	Upsher-Smith Laboratories, LLC	POTASSIUM CHLORIDE	750 mg/1	64000 TABLET, EXTENDED RELEASE in 1 DRUM (24979-230-00)
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)
24979-230-03	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	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-230-03)
24979-229-00	24979-229	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20250601	N/A	ANDA	ANDA218979	Upsher-Smith Laboratories, LLC	POTASSIUM CHLORIDE	600 mg/1	80000 TABLET, EXTENDED RELEASE in 1 DRUM (24979-229-00)
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)
24979-229-03	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	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-229-03)
0245-0835-11	0245-0835	HUMAN PRESCRIPTION DRUG	KLOR-CON	potassium chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250815	N/A	ANDA	ANDA218979	Upsher-Smith Laboratories, LLC	POTASSIUM CHLORIDE	600 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0245-0835-11)
0245-0835-15	0245-0835	HUMAN PRESCRIPTION DRUG	KLOR-CON	potassium chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250815	N/A	ANDA	ANDA218979	Upsher-Smith Laboratories, LLC	POTASSIUM CHLORIDE	600 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0245-0835-15)
42291-487-01	42291-487	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20250808	N/A	ANDA	ANDA218979	AvKARE	POTASSIUM CHLORIDE	750 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-487-01)
42291-487-50	42291-487	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20250808	N/A	ANDA	ANDA218979	AvKARE	POTASSIUM CHLORIDE	750 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-487-50)
0245-0836-11	0245-0836	HUMAN PRESCRIPTION DRUG	KLOR-CON	potassium chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250815	N/A	ANDA	ANDA218979	Upsher-Smith Laboratories, LLC	POTASSIUM CHLORIDE	750 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0245-0836-11)
0245-0836-15	0245-0836	HUMAN PRESCRIPTION DRUG	KLOR-CON	potassium chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250815	N/A	ANDA	ANDA218979	Upsher-Smith Laboratories, LLC	POTASSIUM CHLORIDE	750 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0245-0836-15)