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
71335-2782-4	71335-2782	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20250924	N/A	ANDA	ANDA078853	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2782-4)
71335-2782-1	71335-2782	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20250924	N/A	ANDA	ANDA078853	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2782-1)
0615-8586-39	0615-8586	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20250820	N/A	ANDA	ANDA078853	NCS HealthCare of KY, LLC dba Vangard Labs	DIVALPROEX SODIUM	125 mg/1	30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-8586-39)
0615-8587-39	0615-8587	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20250815	N/A	ANDA	ANDA078853	NCS HealthCare of KY, LLC dba Vangard Labs	DIVALPROEX SODIUM	250 mg/1	30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-8587-39)
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)