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
68788-4079-3	68788-4079	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20260217	N/A	ANDA	ANDA078853	Preferred Pharmaceuticals Inc.	DIVALPROEX SODIUM	250 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-4079-3)
68788-4079-6	68788-4079	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20260217	N/A	ANDA	ANDA078853	Preferred Pharmaceuticals Inc.	DIVALPROEX SODIUM	250 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-4079-6)
68788-4079-9	68788-4079	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20260217	N/A	ANDA	ANDA078853	Preferred Pharmaceuticals Inc.	DIVALPROEX SODIUM	250 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-4079-9)
67046-1647-3	67046-1647	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20240626	N/A	ANDA	ANDA078853	Coupler LLC	DIVALPROEX SODIUM	500 mg/1	30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67046-1647-3)
0615-8588-39	0615-8588	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20250818	N/A	ANDA	ANDA078853	NCS HealthCare of KY, LLC dba Vangard Labs	DIVALPROEX SODIUM	500 mg/1	30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-8588-39)
69452-433-13	69452-433	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20240626	N/A	ANDA	ANDA078853	Bionpharma Inc.	DIVALPROEX SODIUM	125 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-433-13)
69452-433-20	69452-433	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20240626	N/A	ANDA	ANDA078853	Bionpharma Inc.	DIVALPROEX SODIUM	125 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-433-20)
69452-433-30	69452-433	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20240626	N/A	ANDA	ANDA078853	Bionpharma Inc.	DIVALPROEX SODIUM	125 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-433-30)
82804-233-30	82804-233	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20250806	N/A	ANDA	ANDA078853	Proficient Rx LP	DIVALPROEX SODIUM	250 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (82804-233-30)