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
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)
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)
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)
65862-987-01	65862-987	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181219	N/A	ANDA	ANDA210921	Aurobindo Pharma Limited	POTASSIUM CHLORIDE	750 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-987-01)
65862-987-12	65862-987	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181219	N/A	ANDA	ANDA210921	Aurobindo Pharma Limited	POTASSIUM CHLORIDE	750 mg/1	120 BLISTER PACK in 1 CARTON (65862-987-12) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-987-06)
65862-987-80	65862-987	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181219	N/A	ANDA	ANDA210921	Aurobindo Pharma Limited	POTASSIUM CHLORIDE	750 mg/1	80 BLISTER PACK in 1 CARTON (65862-987-80) / 4 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-987-04)
65862-987-99	65862-987	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181219	N/A	ANDA	ANDA210921	Aurobindo Pharma Limited	POTASSIUM CHLORIDE	750 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-987-99)
51655-463-84	51655-463	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20201029	N/A	ANDA	ANDA210921	Northwind Pharmaceuticals, LLC	POTASSIUM CHLORIDE	750 mg/1	14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-463-84)
0904-7216-61	0904-7216	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181219	N/A	ANDA	ANDA210921	Major Pharmaceuticals	POTASSIUM CHLORIDE	750 mg/1	100 BLISTER PACK in 1 CARTON (0904-7216-61) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
68788-8262-3	68788-8262	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220919	N/A	ANDA	ANDA210921	Preferred Pharmaceuticals Inc.	POTASSIUM CHLORIDE	750 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-8262-3)
68788-8262-6	68788-8262	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220919	N/A	ANDA	ANDA210921	Preferred Pharmaceuticals Inc.	POTASSIUM CHLORIDE	750 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-8262-6)
68788-8262-9	68788-8262	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220919	N/A	ANDA	ANDA210921	Preferred Pharmaceuticals Inc.	POTASSIUM CHLORIDE	750 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-8262-9)
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)
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)