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
31722-023-31	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
31722-024-01	31722-024	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20220111	N/A	ANDA	ANDA215939	Camber Pharmaceuticals, Inc.	OXCARBAZEPINE	300 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (31722-024-01)
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)
31722-023-10	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)
31722-023-05	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)
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)
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)
31722-025-10	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
87063-208-60	87063-208	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20260519	N/A	ANDA	ANDA215939	ASCLEMED USA INC.	OXCARBAZEPINE	300 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (87063-208-60)
87063-208-90	87063-208	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20260519	N/A	ANDA	ANDA215939	ASCLEMED USA INC.	OXCARBAZEPINE	300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (87063-208-90)
87063-208-01	87063-208	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20260519	N/A	ANDA	ANDA215939	ASCLEMED USA INC.	OXCARBAZEPINE	300 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (87063-208-01)