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
63629-4698-2	63629-4698	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240521	N/A	ANDA	ANDA202419	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-4698-2)
63629-4698-3	63629-4698	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20140609	N/A	ANDA	ANDA202419	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-4698-3)
63629-4698-1	63629-4698	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240521	N/A	ANDA	ANDA202419	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-4698-1)