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
72162-2371-5	72162-2371	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, EXTENDED RELEASE	ORAL	20240716	N/A	ANDA	ANDA209286	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2371-5)
68788-8358-9	68788-8358	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, EXTENDED RELEASE	ORAL	20230213	N/A	ANDA	ANDA209286	Preferred Pharmaceuticals, Inc.	DIVALPROEX SODIUM	500 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8358-9)
68788-8358-3	68788-8358	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, EXTENDED RELEASE	ORAL	20230213	N/A	ANDA	ANDA209286	Preferred Pharmaceuticals, Inc.	DIVALPROEX SODIUM	500 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8358-3)
68788-8358-6	68788-8358	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, EXTENDED RELEASE	ORAL	20230213	N/A	ANDA	ANDA209286	Preferred Pharmaceuticals, Inc.	DIVALPROEX SODIUM	500 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8358-6)
72189-459-60	72189-459	HUMAN PRESCRIPTION DRUG	Divalproex Sodium ER	Divalproex Sodium ER	TABLET, EXTENDED RELEASE	ORAL	20230403	N/A	ANDA	ANDA209286	Direct_Rx	DIVALPROEX SODIUM	500 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-459-60)