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
57237-106-01	57237-106	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20141024	N/A	ANDA	ANDA090554	Rising Pharma Holdings, Inc.	DIVALPROEX SODIUM	125 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (57237-106-01)
57237-106-05	57237-106	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20141024	N/A	ANDA	ANDA090554	Rising Pharma Holdings, Inc.	DIVALPROEX SODIUM	125 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (57237-106-05)
57237-048-01	57237-048	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20141024	N/A	ANDA	ANDA090554	Rising Pharma Holdings, Inc.	DIVALPROEX SODIUM	500 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (57237-048-01)
57237-048-05	57237-048	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20141024	N/A	ANDA	ANDA090554	Rising Pharma Holdings, Inc.	DIVALPROEX SODIUM	500 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (57237-048-05)
50090-5842-0	50090-5842	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20211103	N/A	ANDA	ANDA090554	A-S Medication Solutions	DIVALPROEX SODIUM	500 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5842-0)
60687-211-21	60687-211	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20160909	N/A	ANDA	ANDA090554	American Health Packaging	DIVALPROEX SODIUM	125 mg/1	30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-211-21) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-211-11)
57237-047-01	57237-047	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20141024	N/A	ANDA	ANDA090554	Rising Pharma Holdings, Inc.	DIVALPROEX SODIUM	250 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (57237-047-01)
57237-047-05	57237-047	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20141024	N/A	ANDA	ANDA090554	Rising Pharma Holdings, Inc.	DIVALPROEX SODIUM	250 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (57237-047-05)
68084-782-61	68084-782	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20160126	N/A	ANDA	ANDA090554	American Health Packaging	DIVALPROEX SODIUM	500 mg/1	90 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-782-61) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (68084-782-11)
68788-8145-3	68788-8145	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20220222	N/A	ANDA	ANDA090554	Preferred Pharmaceuticals Inc.	DIVALPROEX SODIUM	250 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8145-3)
71335-2158-1	71335-2158	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20220811	N/A	ANDA	ANDA090554	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-1)
71335-2158-2	71335-2158	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20230302	N/A	ANDA	ANDA090554	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-2)
71335-2158-3	71335-2158	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20220811	N/A	ANDA	ANDA090554	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-3)
71335-2158-4	71335-2158	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20240403	N/A	ANDA	ANDA090554	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-4)
71335-2158-5	71335-2158	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20220920	N/A	ANDA	ANDA090554	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-5)
68084-776-01	68084-776	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20150302	N/A	ANDA	ANDA090554	American Health Packaging	DIVALPROEX SODIUM	250 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-776-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (68084-776-11)
55154-4679-0	55154-4679	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20150310	N/A	ANDA	ANDA090554	Cardinal Health 107, LLC	DIVALPROEX SODIUM	500 mg/1	10 BLISTER PACK in 1 BAG (55154-4679-0) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
70518-2357-0	70518-2357	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20191010	N/A	ANDA	ANDA090554	REMEDYREPACK INC.	DIVALPROEX SODIUM	500 mg/1	30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2357-0)
70518-2357-1	70518-2357	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20210316	N/A	ANDA	ANDA090554	REMEDYREPACK INC.	DIVALPROEX SODIUM	500 mg/1	100 POUCH in 1 BOX (70518-2357-1) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-2357-2)
70518-2357-5	70518-2357	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20220809	N/A	ANDA	ANDA090554	REMEDYREPACK INC.	DIVALPROEX SODIUM	500 mg/1	30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2357-5)