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
50090-7635-0	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)
62756-798-83	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	30 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-798-83)
62756-798-88	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 (62756-798-88)
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)
62756-797-13	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	500 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-13)
62756-797-18	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	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-18)
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
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)
62756-797-83	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	30 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-83)
62756-797-88	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 (62756-797-88)