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)
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
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)
50090-5335-0	50090-5335	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20201104	N/A	ANDA	ANDA210921	A-S Medication Solutions	POTASSIUM CHLORIDE	750 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5335-0)
50090-5335-1	50090-5335	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20201104	N/A	ANDA	ANDA210921	A-S Medication Solutions	POTASSIUM CHLORIDE	750 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5335-1)
50090-5335-2	50090-5335	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20201104	N/A	ANDA	ANDA210921	A-S Medication Solutions	POTASSIUM CHLORIDE	750 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5335-2)
50090-5335-3	50090-5335	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20201104	N/A	ANDA	ANDA210921	A-S Medication Solutions	POTASSIUM CHLORIDE	750 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5335-3)
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)
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)