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
68382-133-01	68382-133	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130107	N/A	ANDA	ANDA078239	Zydus Pharmaceuticals USA Inc.	DIVALPROEX SODIUM	250 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-133-01)
68382-133-05	68382-133	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130107	N/A	ANDA	ANDA078239	Zydus Pharmaceuticals USA Inc.	DIVALPROEX SODIUM	250 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-133-05)
68382-133-14	68382-133	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130107	N/A	ANDA	ANDA078239	Zydus Pharmaceuticals USA Inc.	DIVALPROEX SODIUM	250 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-133-14)
68382-133-16	68382-133	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130107	N/A	ANDA	ANDA078239	Zydus Pharmaceuticals USA Inc.	DIVALPROEX SODIUM	250 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-133-16)
68382-134-01	68382-134	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130107	N/A	ANDA	ANDA078239	Zydus Pharmaceuticals USA Inc.	DIVALPROEX SODIUM	500 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-134-01)
68382-134-05	68382-134	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130107	N/A	ANDA	ANDA078239	Zydus Pharmaceuticals USA Inc.	DIVALPROEX SODIUM	500 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-134-05)
68382-134-16	68382-134	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130107	N/A	ANDA	ANDA078239	Zydus Pharmaceuticals USA Inc.	DIVALPROEX SODIUM	500 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-134-16)
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)
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)
65841-637-01	65841-637	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130107	N/A	ANDA	ANDA078239	Zydus Lifesciences Limited	DIVALPROEX SODIUM	250 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65841-637-01)
65841-637-05	65841-637	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130107	N/A	ANDA	ANDA078239	Zydus Lifesciences Limited	DIVALPROEX SODIUM	250 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65841-637-05)
65841-637-14	65841-637	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130107	N/A	ANDA	ANDA078239	Zydus Lifesciences Limited	DIVALPROEX SODIUM	250 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65841-637-14)
65841-637-16	65841-637	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130107	N/A	ANDA	ANDA078239	Zydus Lifesciences Limited	DIVALPROEX SODIUM	250 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65841-637-16)
65841-638-01	65841-638	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130107	N/A	ANDA	ANDA078239	Zydus Lifesciences Limited	DIVALPROEX SODIUM	500 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65841-638-01)
65841-638-05	65841-638	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130107	N/A	ANDA	ANDA078239	Zydus Lifesciences Limited	DIVALPROEX SODIUM	500 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65841-638-05)
65841-638-16	65841-638	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130107	N/A	ANDA	ANDA078239	Zydus Lifesciences Limited	DIVALPROEX SODIUM	500 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65841-638-16)
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)