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
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)
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	20260630	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)
60760-698-60	60760-698	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20250513	N/A	ANDA	ANDA090554	ST. MARY'S MEDICAL PARK PHARMACY	DIVALPROEX SODIUM	250 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-698-60)
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)
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)
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)
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)
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	20240906	N/A	ANDA	ANDA090554	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-4)