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
55111-529-78	55111-529	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20080729	N/A	ANDA	ANDA078755	Dr.Reddy's Laboratories Limited	DIVALPROEX SODIUM	125 mg/1	10 BLISTER PACK in 1 CARTON (55111-529-78) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-529-79)
55111-529-30	55111-529	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20080729	N/A	ANDA	ANDA078755	Dr.Reddy's Laboratories Limited	DIVALPROEX SODIUM	125 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-529-30)
55111-530-01	55111-530	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20080729	N/A	ANDA	ANDA078755	Dr.Reddy's Laboratories Limited	DIVALPROEX SODIUM	250 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-530-01)
55111-530-05	55111-530	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20080729	N/A	ANDA	ANDA078755	Dr.Reddy's Laboratories Limited	DIVALPROEX SODIUM	250 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-530-05)
55111-530-30	55111-530	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20080729	N/A	ANDA	ANDA078755	Dr.Reddy's Laboratories Limited	DIVALPROEX SODIUM	250 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-530-30)
55111-529-05	55111-529	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20080729	N/A	ANDA	ANDA078755	Dr.Reddy's Laboratories Limited	DIVALPROEX SODIUM	125 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-529-05)
55111-529-01	55111-529	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20080729	N/A	ANDA	ANDA078755	Dr.Reddy's Laboratories Limited	DIVALPROEX SODIUM	125 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-529-01)
55111-530-78	55111-530	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20080729	N/A	ANDA	ANDA078755	Dr.Reddy's Laboratories Limited	DIVALPROEX SODIUM	250 mg/1	10 BLISTER PACK in 1 CARTON (55111-530-78) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-530-79)
55111-531-78	55111-531	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20080729	N/A	ANDA	ANDA078755	Dr.Reddy's Laboratories Limited	DIVALPROEX SODIUM	500 mg/1	10 BLISTER PACK in 1 CARTON (55111-531-78) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-531-79)
55111-531-01	55111-531	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20080729	N/A	ANDA	ANDA078755	Dr.Reddy's Laboratories Limited	DIVALPROEX SODIUM	500 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-531-01)
55111-531-05	55111-531	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20080729	N/A	ANDA	ANDA078755	Dr.Reddy's Laboratories Limited	DIVALPROEX SODIUM	500 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-531-05)
55111-531-30	55111-531	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20080729	N/A	ANDA	ANDA078755	Dr.Reddy's Laboratories Limited	DIVALPROEX SODIUM	500 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-531-30)