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
71335-1883-1	71335-1883	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, EXTENDED RELEASE	ORAL	20240718	N/A	ANDA	ANDA209286	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1883-1)
71335-1883-2	71335-1883	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, EXTENDED RELEASE	ORAL	20210621	N/A	ANDA	ANDA209286	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1883-2)
71335-1883-3	71335-1883	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, EXTENDED RELEASE	ORAL	20220818	N/A	ANDA	ANDA209286	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1883-3)
68180-261-02	68180-261	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, EXTENDED RELEASE	ORAL	20200918	N/A	ANDA	ANDA209286	Lupin Pharmaceuticals, Inc.	DIVALPROEX SODIUM	500 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-261-02)
68180-261-01	68180-261	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, EXTENDED RELEASE	ORAL	20200918	N/A	ANDA	ANDA209286	Lupin Pharmaceuticals, Inc.	DIVALPROEX SODIUM	500 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-261-01)
68180-260-02	68180-260	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, EXTENDED RELEASE	ORAL	20200918	N/A	ANDA	ANDA209286	Lupin Pharmaceuticals, Inc.	DIVALPROEX SODIUM	250 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-260-02)
70518-3183-0	70518-3183	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, EXTENDED RELEASE	ORAL	20210806	N/A	ANDA	ANDA209286	REMEDYREPACK INC.	DIVALPROEX SODIUM	250 mg/1	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3183-0)
68180-260-01	68180-260	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, EXTENDED RELEASE	ORAL	20200918	N/A	ANDA	ANDA209286	Lupin Pharmaceuticals, Inc.	DIVALPROEX SODIUM	250 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-260-01)
50090-5783-0	50090-5783	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, EXTENDED RELEASE	ORAL	20211008	N/A	ANDA	ANDA209286	A-S Medication Solutions	DIVALPROEX SODIUM	500 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5783-0)
50090-5783-1	50090-5783	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, EXTENDED RELEASE	ORAL	20211008	N/A	ANDA	ANDA209286	A-S Medication Solutions	DIVALPROEX SODIUM	500 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5783-1)
70518-3183-1	70518-3183	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, EXTENDED RELEASE	ORAL	20230730	N/A	ANDA	ANDA209286	REMEDYREPACK INC.	DIVALPROEX SODIUM	250 mg/1	100 POUCH in 1 BOX (70518-3183-1) / 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-3183-2)
70518-3477-1	70518-3477	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, EXTENDED RELEASE	ORAL	20221014	N/A	ANDA	ANDA209286	REMEDYREPACK INC.	DIVALPROEX SODIUM	500 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3477-1)
70518-3477-5	70518-3477	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, EXTENDED RELEASE	ORAL	20230823	N/A	ANDA	ANDA209286	REMEDYREPACK INC.	DIVALPROEX SODIUM	500 mg/1	100 POUCH in 1 BOX (70518-3477-5) / 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-3477-6)
72789-286-60	72789-286	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, EXTENDED RELEASE	ORAL	20221117	N/A	ANDA	ANDA209286	PD-Rx Pharmaceuticals, Inc.	DIVALPROEX SODIUM	250 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-286-60)
0615-8376-39	0615-8376	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, EXTENDED RELEASE	ORAL	20210111	N/A	ANDA	ANDA209286	NCS HealthCare of KY, LLC dba Vangard Labs	DIVALPROEX SODIUM	250 mg/1	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8376-39)
0615-8377-39	0615-8377	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, EXTENDED RELEASE	ORAL	20210203	N/A	ANDA	ANDA209286	NCS HealthCare of KY, LLC dba Vangard Labs	DIVALPROEX SODIUM	500 mg/1	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8377-39)
72162-2371-1	72162-2371	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, EXTENDED RELEASE	ORAL	20240716	N/A	ANDA	ANDA209286	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2371-1)
72162-2371-5	72162-2371	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, EXTENDED RELEASE	ORAL	20240716	N/A	ANDA	ANDA209286	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2371-5)
68788-8358-3	68788-8358	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, EXTENDED RELEASE	ORAL	20230213	N/A	ANDA	ANDA209286	Preferred Pharmaceuticals, Inc.	DIVALPROEX SODIUM	500 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8358-3)
68788-8358-6	68788-8358	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, EXTENDED RELEASE	ORAL	20230213	N/A	ANDA	ANDA209286	Preferred Pharmaceuticals, Inc.	DIVALPROEX SODIUM	500 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8358-6)