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
60429-061-01	60429-061	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20130411	N/A	ANDA	ANDA078069	Golden State Medical Supply, Inc.	OXCARBAZEPINE	150 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (60429-061-01)
60429-061-05	60429-061	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20190910	N/A	ANDA	ANDA078069	Golden State Medical Supply, Inc.	OXCARBAZEPINE	150 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (60429-061-05)
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)
0904-7594-61	0904-7594	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20260403	N/A	ANDA	ANDA078069	Major Pharmaceuticals	OXCARBAZEPINE	300 mg/1	100 BLISTER PACK in 1 CARTON (0904-7594-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
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)
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
70518-2253-0	70518-2253	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20190805	N/A	ANDA	ANDA078069	REMEDYREPACK INC.	OXCARBAZEPINE	150 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2253-0)
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)
51991-293-01	51991-293	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20080111	N/A	ANDA	ANDA078069	Breckenridge Pharmaceutical, Inc.	OXCARBAZEPINE	300 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (51991-293-01)
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)
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
70518-2370-2	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)
0904-7593-61	0904-7593	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20260403	N/A	ANDA	ANDA078069	Major Pharmaceuticals	OXCARBAZEPINE	150 mg/1	100 BLISTER PACK in 1 CARTON (0904-7593-61) / 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)
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)
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)