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
51991-293-05	51991-293	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20080111	N/A	ANDA	ANDA078069	Breckenridge Pharmaceutical, Inc.	OXCARBAZEPINE	300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (51991-293-05)
63629-2075-1	63629-2075	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20080111	N/A	ANDA	ANDA078069	Bryant Ranch Prepack	OXCARBAZEPINE	300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (63629-2075-1)
55154-4323-0	55154-4323	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20230801	N/A	ANDA	ANDA078069	Cardinal Health 107, LLC	OXCARBAZEPINE	150 mg/1	10 BLISTER PACK in 1 BAG (55154-4323-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
0904-7264-61	0904-7264	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20221107	20270228	ANDA	ANDA078069	Major Pharmaceuticals	OXCARBAZEPINE	600 mg/1	100 BLISTER PACK in 1 CARTON (0904-7264-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
63629-3816-1	63629-3816	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20110728	N/A	ANDA	ANDA078069	Bryant Ranch Prepack	OXCARBAZEPINE	150 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63629-3816-1)
63629-3816-2	63629-3816	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20081014	N/A	ANDA	ANDA078069	Bryant Ranch Prepack	OXCARBAZEPINE	150 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63629-3816-2)
63629-3816-3	63629-3816	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20120806	N/A	ANDA	ANDA078069	Bryant Ranch Prepack	OXCARBAZEPINE	150 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63629-3816-3)
63629-6834-1	63629-6834	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20160627	N/A	ANDA	ANDA078069	Bryant Ranch Prepack	OXCARBAZEPINE	600 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63629-6834-1)
63629-6834-2	63629-6834	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20151102	N/A	ANDA	ANDA078069	Bryant Ranch Prepack	OXCARBAZEPINE	600 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63629-6834-2)
63629-6834-3	63629-6834	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20160713	N/A	ANDA	ANDA078069	Bryant Ranch Prepack	OXCARBAZEPINE	600 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63629-6834-3)
71335-0090-1	71335-0090	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20200604	N/A	ANDA	ANDA078069	Bryant Ranch Prepack	OXCARBAZEPINE	300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0090-1)
71335-0090-2	71335-0090	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20200924	N/A	ANDA	ANDA078069	Bryant Ranch Prepack	OXCARBAZEPINE	300 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0090-2)
71335-0090-3	71335-0090	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20200423	N/A	ANDA	ANDA078069	Bryant Ranch Prepack	OXCARBAZEPINE	300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0090-3)
71335-0090-4	71335-0090	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20211123	N/A	ANDA	ANDA078069	Bryant Ranch Prepack	OXCARBAZEPINE	300 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71335-0090-4)
71335-0090-5	71335-0090	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20211123	N/A	ANDA	ANDA078069	Bryant Ranch Prepack	OXCARBAZEPINE	300 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-0090-5)
67046-1597-3	67046-1597	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20250918	N/A	ANDA	ANDA078069	Coupler LLC	OXCARBAZEPINE	150 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1597-3)