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
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)
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
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
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)
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)
70518-4507-0	70518-4507	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20251016	N/A	ANDA	ANDA078069	REMEDYREPACK INC.	OXCARBAZEPINE	300 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4507-0)
70518-4507-1	70518-4507	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20251121	N/A	ANDA	ANDA078069	REMEDYREPACK INC.	OXCARBAZEPINE	300 mg/1	100 POUCH in 1 BOX (70518-4507-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-4507-2)
63629-9186-1	63629-9186	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20220803	N/A	ANDA	ANDA078069	Bryant Ranch Prepack	OXCARBAZEPINE	300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (63629-9186-1)
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)