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
31722-024-05	31722-024	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20230310	N/A	ANDA	ANDA215939	Camber Pharmaceuticals, Inc.	OXCARBAZEPINE	300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (31722-024-05)
31722-024-10	31722-024	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20230310	N/A	ANDA	ANDA215939	Camber Pharmaceuticals, Inc.	OXCARBAZEPINE	300 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (31722-024-10)
31722-024-31	31722-024	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20220111	N/A	ANDA	ANDA215939	Camber Pharmaceuticals, Inc.	OXCARBAZEPINE	300 mg/1	10 BLISTER PACK in 1 CARTON (31722-024-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK
31722-025-01	31722-025	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20220111	N/A	ANDA	ANDA215939	Camber Pharmaceuticals, Inc.	OXCARBAZEPINE	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (31722-025-01)
31722-025-05	31722-025	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20230310	N/A	ANDA	ANDA215939	Camber Pharmaceuticals, Inc.	OXCARBAZEPINE	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (31722-025-05)
31722-025-10	31722-025	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20230310	N/A	ANDA	ANDA215939	Camber Pharmaceuticals, Inc.	OXCARBAZEPINE	600 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (31722-025-10)
31722-025-31	31722-025	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20220111	N/A	ANDA	ANDA215939	Camber Pharmaceuticals, Inc.	OXCARBAZEPINE	600 mg/1	10 BLISTER PACK in 1 CARTON (31722-025-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK
31722-023-01	31722-023	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20220111	N/A	ANDA	ANDA215939	Camber Pharmaceuticals, Inc.	OXCARBAZEPINE	150 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (31722-023-01)
31722-023-05	31722-023	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20230310	N/A	ANDA	ANDA215939	Camber Pharmaceuticals, Inc.	OXCARBAZEPINE	150 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (31722-023-05)
60687-733-01	60687-733	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20230127	N/A	ANDA	ANDA215939	American Health Packaging	OXCARBAZEPINE	600 mg/1	100 BLISTER PACK in 1 CARTON (60687-733-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-733-11)
31722-023-31	31722-023	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20220111	N/A	ANDA	ANDA215939	Camber Pharmaceuticals, Inc.	OXCARBAZEPINE	150 mg/1	10 BLISTER PACK in 1 CARTON (31722-023-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK
60687-711-01	60687-711	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20230202	N/A	ANDA	ANDA215939	American Health Packaging	OXCARBAZEPINE	150 mg/1	100 BLISTER PACK in 1 CARTON (60687-711-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-711-11)
60687-722-01	60687-722	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20230124	N/A	ANDA	ANDA215939	American Health Packaging	OXCARBAZEPINE	300 mg/1	100 BLISTER PACK in 1 CARTON (60687-722-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-722-11)
0615-8567-39	0615-8567	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20250221	N/A	ANDA	ANDA215939	NCS HealthCare of KY, LLC dba Vangard Labs	OXCARBAZEPINE	600 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8567-39)
0615-8447-39	0615-8447	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20230113	N/A	ANDA	ANDA215939	NCS HealthCare of KY, LLC dba Vangard Labs	OXCARBAZEPINE	150 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8447-39)
0615-8448-39	0615-8448	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20230113	N/A	ANDA	ANDA215939	NCS HealthCare of KY, LLC dba Vangard Labs	OXCARBAZEPINE	300 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8448-39)
70518-3925-0	70518-3925	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20231126	N/A	ANDA	ANDA215939	REMEDYREPACK INC.	OXCARBAZEPINE	600 mg/1	100 POUCH in 1 BOX (70518-3925-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-3925-1)
70518-3921-0	70518-3921	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20231122	N/A	ANDA	ANDA215939	REMEDYREPACK INC.	OXCARBAZEPINE	300 mg/1	100 POUCH in 1 BOX (70518-3921-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-3921-1)
70518-3940-0	70518-3940	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20231206	N/A	ANDA	ANDA215939	REMEDYREPACK INC.	OXCARBAZEPINE	150 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3940-0)
70518-3940-1	70518-3940	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20240224	N/A	ANDA	ANDA215939	REMEDYREPACK INC.	OXCARBAZEPINE	150 mg/1	100 POUCH in 1 BOX (70518-3940-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-3940-2)