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
71335-2548-1	71335-2548	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20250121	N/A	ANDA	ANDA215939	Bryant Ranch Prepack	OXCARBAZEPINE	300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2548-1)
71335-2548-2	71335-2548	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20250121	N/A	ANDA	ANDA215939	Bryant Ranch Prepack	OXCARBAZEPINE	300 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-2548-2)
71335-2548-3	71335-2548	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20250121	N/A	ANDA	ANDA215939	Bryant Ranch Prepack	OXCARBAZEPINE	300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-2548-3)
71335-2548-4	71335-2548	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20250121	N/A	ANDA	ANDA215939	Bryant Ranch Prepack	OXCARBAZEPINE	300 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71335-2548-4)
71335-2548-5	71335-2548	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20250121	N/A	ANDA	ANDA215939	Bryant Ranch Prepack	OXCARBAZEPINE	300 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-2548-5)
50268-679-15	50268-679	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20230607	N/A	ANDA	ANDA215939	AvPAK	OXCARBAZEPINE	150 mg/1	50 BLISTER PACK in 1 BOX (50268-679-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-679-11)
50268-680-15	50268-680	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20230607	N/A	ANDA	ANDA215939	AvPAK	OXCARBAZEPINE	300 mg/1	50 BLISTER PACK in 1 BOX (50268-680-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-680-11)
50268-681-15	50268-681	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20230607	N/A	ANDA	ANDA215939	AvPAK	OXCARBAZEPINE	600 mg/1	50 BLISTER PACK in 1 BOX (50268-681-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-681-11)
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)
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)
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)
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)
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)
31722-023-10	31722-023	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20230310	N/A	ANDA	ANDA215939	Camber Pharmaceuticals, Inc.	OXCARBAZEPINE	150 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (31722-023-10)
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
72865-283-01	72865-283	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20240718	N/A	ANDA	ANDA215939	XLCare Pharmaceuticals Inc.	OXCARBAZEPINE	150 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72865-283-01)
72865-285-01	72865-285	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20240718	N/A	ANDA	ANDA215939	XLCare Pharmaceuticals Inc.	OXCARBAZEPINE	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72865-285-01)
72865-285-05	72865-285	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20240718	N/A	ANDA	ANDA215939	XLCare Pharmaceuticals Inc.	OXCARBAZEPINE	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72865-285-05)