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
65862-959-05	65862-959	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20141024	N/A	ANDA	ANDA090554	Aurobindo Pharma Limited	DIVALPROEX SODIUM	125 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-959-05)
65862-959-10	65862-959	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20141024	N/A	ANDA	ANDA090554	Aurobindo Pharma Limited	DIVALPROEX SODIUM	125 mg/1	10 BLISTER PACK in 1 CARTON (65862-959-10) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK
65862-959-71	65862-959	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20141024	N/A	ANDA	ANDA090554	Aurobindo Pharma Limited	DIVALPROEX SODIUM	125 mg/1	7000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-959-71)
65862-959-99	65862-959	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20141024	N/A	ANDA	ANDA090554	Aurobindo Pharma Limited	DIVALPROEX SODIUM	125 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-959-99)