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
71610-944-30	71610-944	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250903	N/A	ANDA	ANDA210921	Aphena Pharma Solutions - Tennessee, LLC	POTASSIUM CHLORIDE	750 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-944-30)
71610-944-53	71610-944	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250903	N/A	ANDA	ANDA210921	Aphena Pharma Solutions - Tennessee, LLC	POTASSIUM CHLORIDE	750 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-944-53)
71610-944-60	71610-944	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250903	N/A	ANDA	ANDA210921	Aphena Pharma Solutions - Tennessee, LLC	POTASSIUM CHLORIDE	750 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-944-60)
71610-944-70	71610-944	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250903	N/A	ANDA	ANDA210921	Aphena Pharma Solutions - Tennessee, LLC	POTASSIUM CHLORIDE	750 mg/1	120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-944-70)
70518-2964-0	70518-2964	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20201209	N/A	ANDA	ANDA210921	REMEDYREPACK INC.	POTASSIUM CHLORIDE	750 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-2964-0)
70518-2964-3	70518-2964	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240312	N/A	ANDA	ANDA210921	REMEDYREPACK INC.	POTASSIUM CHLORIDE	750 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2964-3)
70518-2964-4	70518-2964	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250325	N/A	ANDA	ANDA210921	REMEDYREPACK INC.	POTASSIUM CHLORIDE	750 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2964-4)
68001-518-00	68001-518	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20210910	N/A	ANDA	ANDA210921	BluePoint Laboratories	POTASSIUM CHLORIDE	750 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-518-00)
68001-518-08	68001-518	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20210910	N/A	ANDA	ANDA210921	BluePoint Laboratories	POTASSIUM CHLORIDE	750 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-518-08)
65862-986-01	65862-986	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181219	N/A	ANDA	ANDA210921	Aurobindo Pharma Limited	POTASSIUM CHLORIDE	600 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-986-01)
65862-986-05	65862-986	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181219	N/A	ANDA	ANDA210921	Aurobindo Pharma Limited	POTASSIUM CHLORIDE	600 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-986-05)
65862-986-12	65862-986	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181219	N/A	ANDA	ANDA210921	Aurobindo Pharma Limited	POTASSIUM CHLORIDE	600 mg/1	120 BLISTER PACK in 1 CARTON (65862-986-12) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-986-06)
65862-986-80	65862-986	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181219	N/A	ANDA	ANDA210921	Aurobindo Pharma Limited	POTASSIUM CHLORIDE	600 mg/1	80 BLISTER PACK in 1 CARTON (65862-986-80) / 4 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-986-04)
60687-810-09	60687-810	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240120	N/A	ANDA	ANDA210921	American Health Packaging	POTASSIUM CHLORIDE	750 mg/1	80 BLISTER PACK in 1 CARTON (60687-810-09) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-810-11)
63629-2620-1	63629-2620	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240206	N/A	ANDA	ANDA210921	Bryant Ranch Prepack	POTASSIUM CHLORIDE	600 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-1)
63629-2620-2	63629-2620	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240206	N/A	ANDA	ANDA210921	Bryant Ranch Prepack	POTASSIUM CHLORIDE	600 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-2)
63629-2620-3	63629-2620	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240206	N/A	ANDA	ANDA210921	Bryant Ranch Prepack	POTASSIUM CHLORIDE	600 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-3)
63629-2620-4	63629-2620	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240206	N/A	ANDA	ANDA210921	Bryant Ranch Prepack	POTASSIUM CHLORIDE	600 mg/1	180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-4)
63629-2620-5	63629-2620	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240206	N/A	ANDA	ANDA210921	Bryant Ranch Prepack	POTASSIUM CHLORIDE	600 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-5)
63629-2620-6	63629-2620	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240206	N/A	ANDA	ANDA210921	Bryant Ranch Prepack	POTASSIUM CHLORIDE	600 mg/1	20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-6)