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
63629-4278-1	63629-4278	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20211222	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-4278-1)
63629-4278-2	63629-4278	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20121119	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-4278-2)
63629-4278-3	63629-4278	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20141110	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-4278-3)
63629-4278-4	63629-4278	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20180531	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	180 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-4278-4)
63629-4278-5	63629-4278	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20180917	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	120 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-4278-5)
63187-742-30	63187-742	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20161003	N/A	ANDA	ANDA079163	Proficient Rx LP	DIVALPROEX SODIUM	250 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-742-30)
63187-742-60	63187-742	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20161003	N/A	ANDA	ANDA079163	Proficient Rx LP	DIVALPROEX SODIUM	250 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-742-60)
63187-742-90	63187-742	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20161003	N/A	ANDA	ANDA079163	Proficient Rx LP	DIVALPROEX SODIUM	250 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-742-90)
70518-4575-0	70518-4575	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20260217	N/A	ANDA	ANDA079163	REMEDYREPACK INC.	DIVALPROEX SODIUM	500 mg/1	30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-4575-0)
60687-857-21	60687-857	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20250317	N/A	ANDA	ANDA079163	American Health Packaging	DIVALPROEX SODIUM	125 mg/1	30 BLISTER PACK in 1 CARTON (60687-857-21) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-857-11)
63187-743-30	63187-743	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20161003	N/A	ANDA	ANDA079163	Proficient Rx LP	DIVALPROEX SODIUM	500 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-743-30)
63187-743-60	63187-743	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20161003	N/A	ANDA	ANDA079163	Proficient Rx LP	DIVALPROEX SODIUM	500 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-743-60)
63187-743-90	63187-743	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20161003	N/A	ANDA	ANDA079163	Proficient Rx LP	DIVALPROEX SODIUM	500 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-743-90)
72162-2460-1	72162-2460	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20250221	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	250 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2460-1)
72162-2460-3	72162-2460	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20250221	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	250 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2460-3)
72162-2460-5	72162-2460	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20250221	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	250 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2460-5)
50090-2007-0	50090-2007	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20150918	N/A	ANDA	ANDA079163	A-S Medication Solutions	DIVALPROEX SODIUM	250 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-2007-0)
50090-2007-1	50090-2007	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20170802	N/A	ANDA	ANDA079163	A-S Medication Solutions	DIVALPROEX SODIUM	250 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-2007-1)
60687-868-01	60687-868	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20250321	N/A	ANDA	ANDA079163	American Health Packaging	DIVALPROEX SODIUM	250 mg/1	100 BLISTER PACK in 1 CARTON (60687-868-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-868-11)
71335-0008-1	71335-0008	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20181221	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	250 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-1)