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
70934-948-60	70934-948	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20220203	20240531	ANDA	ANDA079163	Denton Pharma, Inc. DBA Northwind Pharmaceuticals	DIVALPROEX SODIUM	500 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70934-948-60)
70934-949-60	70934-949	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20220209	20240630	ANDA	ANDA079163	Denton Pharma, Inc. DBA Northwind Pharmaceuticals	DIVALPROEX SODIUM	250 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70934-949-60)
70518-2017-2	70518-2017	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20230130	N/A	ANDA	ANDA079163	REMEDYREPACK INC.	DIVALPROEX SODIUM	125 mg/1	30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2017-2)
61919-249-60	61919-249	HUMAN PRESCRIPTION DRUG	DIVALPROEX SODIUM	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20220406	N/A	ANDA	ANDA079163	DirectRx	DIVALPROEX SODIUM	500 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-249-60)