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
72789-353-01	72789-353	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20231018	N/A	ANDA	ANDA078597	PD-Rx Pharmaceuticals, Inc.	DIVALPROEX SODIUM	250 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-353-01)
72789-354-01	72789-354	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20231017	N/A	ANDA	ANDA078597	PD-Rx Pharmaceuticals, Inc.	DIVALPROEX SODIUM	500 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-354-01)
50090-7635-0	50090-7635	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20250818	N/A	ANDA	ANDA078597	A-S Medication Solutions	DIVALPROEX SODIUM	125 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7635-0)
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)
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)
70518-1558-0	70518-1558	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20181019	N/A	ANDA	ANDA078597	REMEDYREPACK INC.	DIVALPROEX SODIUM	500 mg/1	30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-1558-0)
70518-1558-1	70518-1558	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20191016	N/A	ANDA	ANDA078597	REMEDYREPACK INC.	DIVALPROEX SODIUM	500 mg/1	100 POUCH in 1 BOX (70518-1558-1) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-1558-2)
55154-2336-0	55154-2336	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20080729	N/A	ANDA	ANDA078597	Cardinal Health 107, LLC	DIVALPROEX SODIUM	500 mg/1	10 BLISTER PACK in 1 BAG (55154-2336-0) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
70518-2674-0	70518-2674	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20200406	N/A	ANDA	ANDA078597	REMEDYREPACK INC.	DIVALPROEX SODIUM	500 mg/1	100 POUCH in 1 BOX (70518-2674-0) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-2674-1)
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)
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
70518-3431-0	70518-3431	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20220603	N/A	ANDA	ANDA078597	REMEDYREPACK INC.	DIVALPROEX SODIUM	250 mg/1	60 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3431-0)
70518-3431-2	70518-3431	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20220628	N/A	ANDA	ANDA078597	REMEDYREPACK INC.	DIVALPROEX SODIUM	250 mg/1	100 POUCH in 1 BOX (70518-3431-2) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-3431-3)
67046-1571-3	67046-1571	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20250702	N/A	ANDA	ANDA078597	Coupler LLC	DIVALPROEX SODIUM	250 mg/1	30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67046-1571-3)
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)
62756-796-18	62756-796	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20080729	N/A	ANDA	ANDA078597	Sun Pharmaceutical Industries, Inc.	DIVALPROEX SODIUM	125 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-796-18)
62756-796-88	62756-796	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20080729	N/A	ANDA	ANDA078597	Sun Pharmaceutical Industries, Inc.	DIVALPROEX SODIUM	125 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-796-88)
62756-797-08	62756-797	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20080729	N/A	ANDA	ANDA078597	Sun Pharmaceutical Industries, Inc.	DIVALPROEX SODIUM	250 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-08)