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
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)
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)
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)
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)
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)
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)
60760-798-60	60760-798	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20250513	N/A	ANDA	ANDA078597	ST. MARY'S MEDICAL PARK PHARMACY	DIVALPROEX SODIUM	500 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-798-60)
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)
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
62756-796-08	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 (62756-796-08)
62756-796-13	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	500 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-796-13)
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)
62756-796-83	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	30 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-796-83)
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)