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
55111-534-01	55111-534	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20130811	N/A	ANDA	ANDA090070	Dr. Reddy's Laboratories Ltd	DIVALPROEX SODIUM	500 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-534-01)
55111-534-05	55111-534	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20130811	N/A	ANDA	ANDA090070	Dr. Reddy's Laboratories Ltd	DIVALPROEX SODIUM	500 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-534-05)
55111-534-30	55111-534	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20130811	N/A	ANDA	ANDA090070	Dr. Reddy's Laboratories Ltd	DIVALPROEX SODIUM	500 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-534-30)
55111-534-60	55111-534	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20130811	N/A	ANDA	ANDA090070	Dr. Reddy's Laboratories Ltd	DIVALPROEX SODIUM	500 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-534-60)
68788-4100-3	68788-4100	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20260420	N/A	ANDA	ANDA090070	Preferred Pharmaceuticals Inc.	DIVALPROEX SODIUM	500 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-4100-3)
68788-4100-6	68788-4100	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20260420	N/A	ANDA	ANDA090070	Preferred Pharmaceuticals Inc.	DIVALPROEX SODIUM	500 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-4100-6)
68788-4100-9	68788-4100	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20260420	N/A	ANDA	ANDA090070	Preferred Pharmaceuticals Inc.	DIVALPROEX SODIUM	500 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-4100-9)