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
65841-635-05	65841-635	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20100306	N/A	ANDA	ANDA077100	Zydus Lifesciences Limited	DIVALPROEX SODIUM	250 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (65841-635-05)
65841-636-01	65841-636	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20100306	N/A	ANDA	ANDA077100	Zydus Lifesciences Limited	DIVALPROEX SODIUM	500 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (65841-636-01)
65841-636-05	65841-636	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20100306	N/A	ANDA	ANDA077100	Zydus Lifesciences Limited	DIVALPROEX SODIUM	500 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (65841-636-05)
65841-635-01	65841-635	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20100306	N/A	ANDA	ANDA077100	Zydus Lifesciences Limited	DIVALPROEX SODIUM	250 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (65841-635-01)
65841-634-05	65841-634	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20100306	N/A	ANDA	ANDA077100	Zydus Lifesciences Limited	DIVALPROEX SODIUM	125 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (65841-634-05)
65841-634-01	65841-634	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20100306	N/A	ANDA	ANDA077100	Zydus Lifesciences Limited	DIVALPROEX SODIUM	125 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (65841-634-01)
68382-031-01	68382-031	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20100306	N/A	ANDA	ANDA077100	Zydus Pharmaceuticals (USA) Inc.	DIVALPROEX SODIUM	125 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-031-01)
68382-033-01	68382-033	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20100306	N/A	ANDA	ANDA077100	Zydus Pharmaceuticals (USA) Inc.	DIVALPROEX SODIUM	500 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-033-01)
68382-033-05	68382-033	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20100306	N/A	ANDA	ANDA077100	Zydus Pharmaceuticals (USA) Inc.	DIVALPROEX SODIUM	500 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-033-05)
68382-031-05	68382-031	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20100306	N/A	ANDA	ANDA077100	Zydus Pharmaceuticals (USA) Inc.	DIVALPROEX SODIUM	125 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-031-05)
68382-032-01	68382-032	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20100306	N/A	ANDA	ANDA077100	Zydus Pharmaceuticals (USA) Inc.	DIVALPROEX SODIUM	250 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-032-01)
68382-032-05	68382-032	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20100306	N/A	ANDA	ANDA077100	Zydus Pharmaceuticals (USA) Inc.	DIVALPROEX SODIUM	250 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-032-05)