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
55154-4154-0	55154-4154	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20080729	N/A	ANDA	ANDA078597	Cardinal Health 107, LLC	DIVALPROEX SODIUM	250 mg/1	10 BLISTER PACK in 1 BAG (55154-4154-0) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
0904-6861-61	0904-6861	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20080729	N/A	ANDA	ANDA078597	Major Pharmaceuticals	DIVALPROEX SODIUM	500 mg/1	100 BLISTER PACK in 1 CARTON (0904-6861-61) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
0904-6861-90	0904-6861	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20080729	N/A	ANDA	ANDA078597	Major Pharmaceuticals	DIVALPROEX SODIUM	500 mg/1	90 BLISTER PACK in 1 CARTON (0904-6861-90) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
50090-1123-0	50090-1123	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20141128	N/A	ANDA	ANDA078597	A-S Medication Solutions	DIVALPROEX SODIUM	250 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-1123-0)
50090-1123-1	50090-1123	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20241024	N/A	ANDA	ANDA078597	A-S Medication Solutions	DIVALPROEX SODIUM	250 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-1123-1)
70518-2674-2	70518-2674	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20210430	N/A	ANDA	ANDA078597	REMEDYREPACK INC.	DIVALPROEX SODIUM	500 mg/1	30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2674-2)
71335-2344-1	71335-2344	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20240530	N/A	ANDA	ANDA078597	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-1)
71335-2344-2	71335-2344	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20240530	N/A	ANDA	ANDA078597	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-2)
17856-0797-1	17856-0797	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20181102	N/A	ANDA	ANDA078597	ATLANTIC BIOLOGICALS CORP.	DIVALPROEX SODIUM	250 mg/1	100 POUCH in 1 BOX, UNIT-DOSE (17856-0797-1) / 1 TABLET, DELAYED RELEASE in 1 POUCH
0904-6860-61	0904-6860	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20080729	N/A	ANDA	ANDA078597	Major Pharmaceuticals	DIVALPROEX SODIUM	250 mg/1	100 BLISTER PACK in 1 CARTON (0904-6860-61) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
72162-2316-1	72162-2316	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20240516	N/A	ANDA	ANDA078597	Bryant Ranch Prepack	DIVALPROEX SODIUM	250 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2316-1)
72162-2316-5	72162-2316	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20240516	N/A	ANDA	ANDA078597	Bryant Ranch Prepack	DIVALPROEX SODIUM	250 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2316-5)
72189-636-60	72189-636	HUMAN PRESCRIPTION DRUG	Divalproex Sodium D/R	Divalproex Sodium D/R	TABLET, DELAYED RELEASE	ORAL	20250728	N/A	ANDA	ANDA078597	Direct_Rx	DIVALPROEX SODIUM	250 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-636-60)
71335-2277-1	71335-2277	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20231129	N/A	ANDA	ANDA078597	Bryant Ranch Prepack	DIVALPROEX SODIUM	250 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2277-1)
71335-2277-2	71335-2277	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20240530	N/A	ANDA	ANDA078597	Bryant Ranch Prepack	DIVALPROEX SODIUM	250 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2277-2)
71335-2277-3	71335-2277	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20240530	N/A	ANDA	ANDA078597	Bryant Ranch Prepack	DIVALPROEX SODIUM	250 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2277-3)
71335-2344-3	71335-2344	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20240129	N/A	ANDA	ANDA078597	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-3)
71335-2344-4	71335-2344	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20240530	N/A	ANDA	ANDA078597	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-4)
71335-2344-5	71335-2344	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20240530	N/A	ANDA	ANDA078597	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-5)
62756-798-08	62756-798	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20080729	N/A	ANDA	ANDA078597	Sun Pharmaceutical Industries, Inc.	DIVALPROEX SODIUM	500 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-798-08)