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
68001-105-00	68001-105	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20131008	N/A	ANDA	ANDA078239	BluePoint Laboratories	DIVALPROEX SODIUM	250 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-105-00)
68001-105-03	68001-105	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20131008	N/A	ANDA	ANDA078239	BluePoint Laboratories	DIVALPROEX SODIUM	250 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-105-03)
67046-1137-3	67046-1137	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241108	N/A	ANDA	ANDA078239	Coupler LLC	DIVALPROEX SODIUM	250 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (67046-1137-3)
68084-310-01	68084-310	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20131121	N/A	ANDA	ANDA078239	American Health Packaging	DIVALPROEX SODIUM	250 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-310-01) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-310-11)
68084-415-01	68084-415	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20131121	N/A	ANDA	ANDA078239	American Health Packaging	DIVALPROEX SODIUM	500 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-415-01) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-415-11)
68084-415-02	68084-415	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230206	20260630	ANDA	ANDA078239	American Health Packaging	DIVALPROEX SODIUM	500 mg/1	80 BLISTER PACK in 1 CARTON (68084-415-02) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-415-93)
68001-106-00	68001-106	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20131008	N/A	ANDA	ANDA078239	BluePoint Laboratories	DIVALPROEX SODIUM	500 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-106-00)
68001-106-03	68001-106	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20131008	N/A	ANDA	ANDA078239	BluePoint Laboratories	DIVALPROEX SODIUM	500 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-106-03)