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
60760-798-60	60760-798	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20250513	N/A	ANDA	ANDA078597	ST. MARY'S MEDICAL PARK PHARMACY	DIVALPROEX SODIUM	500 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-798-60)
68071-3553-6	68071-3553	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20231207	N/A	ANDA	ANDA078597	NuCare Pharmaceuticals,Inc.	DIVALPROEX SODIUM	250 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3553-6)
68788-8609-9	68788-8609	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20250328	N/A	ANDA	ANDA078597	Preferred Pharmaceuticals Inc.	DIVALPROEX SODIUM	250 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8609-9)
68788-8609-6	68788-8609	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20250328	N/A	ANDA	ANDA078597	Preferred Pharmaceuticals Inc.	DIVALPROEX SODIUM	250 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8609-6)
68788-8609-3	68788-8609	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20250328	N/A	ANDA	ANDA078597	Preferred Pharmaceuticals Inc.	DIVALPROEX SODIUM	250 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8609-3)
71335-2277-2	71335-2277	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20240530	N/A	ANDA	ANDA078597	Bryant Ranch Prepack	DIVALPROEX SODIUM	250 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2277-2)
71335-2277-3	71335-2277	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20240530	N/A	ANDA	ANDA078597	Bryant Ranch Prepack	DIVALPROEX SODIUM	250 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2277-3)
71335-2344-1	71335-2344	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20240530	N/A	ANDA	ANDA078597	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-1)
71335-2344-2	71335-2344	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20240530	N/A	ANDA	ANDA078597	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-2)
71335-2344-3	71335-2344	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20240129	N/A	ANDA	ANDA078597	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-3)
71335-2344-4	71335-2344	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20240530	N/A	ANDA	ANDA078597	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-4)
71335-2344-5	71335-2344	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20240530	N/A	ANDA	ANDA078597	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-5)
50090-1123-0	50090-1123	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20141128	N/A	ANDA	ANDA078597	A-S Medication Solutions	DIVALPROEX SODIUM	250 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-1123-0)
50090-1123-1	50090-1123	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20241024	N/A	ANDA	ANDA078597	A-S Medication Solutions	DIVALPROEX SODIUM	250 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-1123-1)
72162-2316-1	72162-2316	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20240516	N/A	ANDA	ANDA078597	Bryant Ranch Prepack	DIVALPROEX SODIUM	250 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2316-1)
72162-2316-5	72162-2316	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20240516	N/A	ANDA	ANDA078597	Bryant Ranch Prepack	DIVALPROEX SODIUM	250 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2316-5)
71335-2277-4	71335-2277	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20240530	N/A	ANDA	ANDA078597	Bryant Ranch Prepack	DIVALPROEX SODIUM	250 mg/1	120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2277-4)
71335-2277-1	71335-2277	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20231129	N/A	ANDA	ANDA078597	Bryant Ranch Prepack	DIVALPROEX SODIUM	250 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2277-1)
50090-7635-0	50090-7635	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20250818	N/A	ANDA	ANDA078597	A-S Medication Solutions	DIVALPROEX SODIUM	125 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7635-0)
72789-353-01	72789-353	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20231018	N/A	ANDA	ANDA078597	PD-Rx Pharmaceuticals, Inc.	DIVALPROEX SODIUM	250 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-353-01)