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
0904-7262-61	0904-7262	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20221107	N/A	ANDA	ANDA078069	Major Pharmaceuticals	OXCARBAZEPINE	150 mg/1	100 BLISTER PACK in 1 CARTON (0904-7262-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
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
68788-7866-9	68788-7866	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20210215	N/A	ANDA	ANDA078069	Preferred Pharmaceuticals Inc.	OXCARBAZEPINE	600 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-7866-9)
51991-053-01	51991-053	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20250129	N/A	ANDA	ANDA078069	Breckenridge Pharmaceutical, Inc.	OXCARBAZEPINE	150 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (51991-053-01)
51991-053-05	51991-053	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20250129	N/A	ANDA	ANDA078069	Breckenridge Pharmaceutical, Inc.	OXCARBAZEPINE	150 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (51991-053-05)
70518-4480-0	70518-4480	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20250913	N/A	ANDA	ANDA078069	REMEDYREPACK INC.	OXCARBAZEPINE	150 mg/1	100 POUCH in 1 BOX (70518-4480-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4480-1)
70518-4480-2	70518-4480	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20251024	N/A	ANDA	ANDA078069	REMEDYREPACK INC.	OXCARBAZEPINE	150 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4480-2)
70518-2370-2	70518-2370	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20241004	N/A	ANDA	ANDA078069	REMEDYREPACK INC.	OXCARBAZEPINE	300 mg/1	100 POUCH in 1 BOX (70518-2370-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-2370-3)
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
63629-2075-1	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)
70518-4465-0	70518-4465	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20250904	N/A	ANDA	ANDA078069	REMEDYREPACK INC.	OXCARBAZEPINE	600 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4465-0)
70518-4465-1	70518-4465	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20251012	N/A	ANDA	ANDA078069	REMEDYREPACK INC.	OXCARBAZEPINE	600 mg/1	100 POUCH in 1 BOX (70518-4465-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-4465-2)
0904-7263-61	0904-7263	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20221107	N/A	ANDA	ANDA078069	Major Pharmaceuticals	OXCARBAZEPINE	300 mg/1	100 BLISTER PACK in 1 CARTON (0904-7263-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
51991-055-01	51991-055	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20250129	N/A	ANDA	ANDA078069	Breckenridge Pharmaceutical, Inc.	OXCARBAZEPINE	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (51991-055-01)
51991-055-05	51991-055	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20250129	N/A	ANDA	ANDA078069	Breckenridge Pharmaceutical, Inc.	OXCARBAZEPINE	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (51991-055-05)
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