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
68084-867-01	68084-867	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20141203	20240630	ANDA	ANDA078069	American Health Packaging	OXCARBAZEPINE	600 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-867-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-867-11)
70518-2253-1	70518-2253	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20210803	N/A	ANDA	ANDA078069	REMEDYREPACK INC.	OXCARBAZEPINE	150 mg/1	100 POUCH in 1 BOX (70518-2253-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-2253-2)
70518-2254-0	70518-2254	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20190805	N/A	ANDA	ANDA078069	REMEDYREPACK INC.	OXCARBAZEPINE	600 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2254-0)
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)
70518-2276-0	70518-2276	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20190822	N/A	ANDA	ANDA078069	REMEDYREPACK INC.	OXCARBAZEPINE	300 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2276-0)
55154-4320-0	55154-4320	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20230801	N/A	ANDA	ANDA078069	Cardinal Health 107, LLC	OXCARBAZEPINE	300 mg/1	10 BLISTER PACK in 1 BAG (55154-4320-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
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)
55154-8187-0	55154-8187	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20141104	N/A	ANDA	ANDA078069	Cardinal Health 107, LLC	OXCARBAZEPINE	150 mg/1	10 BLISTER PACK in 1 BAG (55154-8187-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
55154-8198-0	55154-8198	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20141105	N/A	ANDA	ANDA078069	Cardinal Health 107, LLC	OXCARBAZEPINE	300 mg/1	10 BLISTER PACK in 1 BAG (55154-8198-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
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
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)
51991-292-01	51991-292	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20080111	N/A	ANDA	ANDA078069	Breckenridge Pharmaceutical, Inc.	OXCARBAZEPINE	150 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (51991-292-01)
51991-292-05	51991-292	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20080111	N/A	ANDA	ANDA078069	Breckenridge Pharmaceutical, Inc.	OXCARBAZEPINE	150 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (51991-292-05)
51991-294-05	51991-294	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20080111	N/A	ANDA	ANDA078069	Breckenridge Pharmaceutical, Inc.	OXCARBAZEPINE	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (51991-294-05)
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)