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
55154-4679-0	55154-4679	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20160126	20260630	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
70518-3683-0	70518-3683	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20230317	N/A	ANDA	ANDA090554	REMEDYREPACK INC.	DIVALPROEX SODIUM	125 mg/1	30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3683-0)
70518-3683-1	70518-3683	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20230913	N/A	ANDA	ANDA090554	REMEDYREPACK INC.	DIVALPROEX SODIUM	125 mg/1	30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3683-1)
70518-3683-2	70518-3683	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20250701	N/A	ANDA	ANDA090554	REMEDYREPACK INC.	DIVALPROEX SODIUM	125 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-3683-2)
50090-7121-0	50090-7121	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20240327	N/A	ANDA	ANDA090554	A-S Medication Solutions	DIVALPROEX SODIUM	125 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7121-0)
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)
65862-402-01	65862-402	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20141024	N/A	ANDA	ANDA090554	Aurobindo Pharma Limited	DIVALPROEX SODIUM	250 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-402-01)
65862-402-05	65862-402	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20141024	N/A	ANDA	ANDA090554	Aurobindo Pharma Limited	DIVALPROEX SODIUM	250 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-402-05)
65862-402-10	65862-402	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20141024	N/A	ANDA	ANDA090554	Aurobindo Pharma Limited	DIVALPROEX SODIUM	250 mg/1	10 BLISTER PACK in 1 CARTON (65862-402-10) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK
65862-402-39	65862-402	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20141024	N/A	ANDA	ANDA090554	Aurobindo Pharma Limited	DIVALPROEX SODIUM	250 mg/1	3000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-402-39)
65862-402-99	65862-402	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20141024	N/A	ANDA	ANDA090554	Aurobindo Pharma Limited	DIVALPROEX SODIUM	250 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-402-99)
68084-776-01	68084-776	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20150302	20260630	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)
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)
65862-959-01	65862-959	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20141024	N/A	ANDA	ANDA090554	Aurobindo Pharma Limited	DIVALPROEX SODIUM	125 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-959-01)
65862-959-05	65862-959	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20141024	N/A	ANDA	ANDA090554	Aurobindo Pharma Limited	DIVALPROEX SODIUM	125 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-959-05)
65862-959-10	65862-959	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20141024	N/A	ANDA	ANDA090554	Aurobindo Pharma Limited	DIVALPROEX SODIUM	125 mg/1	10 BLISTER PACK in 1 CARTON (65862-959-10) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK
65862-959-71	65862-959	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20141024	N/A	ANDA	ANDA090554	Aurobindo Pharma Limited	DIVALPROEX SODIUM	125 mg/1	7000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-959-71)
65862-959-99	65862-959	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20141024	N/A	ANDA	ANDA090554	Aurobindo Pharma Limited	DIVALPROEX SODIUM	125 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-959-99)
60687-211-21	60687-211	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20160909	20260228	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)