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
31722-024-10	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)
72603-272-01	72603-272	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20240901	N/A	ANDA	ANDA215939	NorthStar RxLLC	OXCARBAZEPINE	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72603-272-01)
72603-272-02	72603-272	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20250428	N/A	ANDA	ANDA215939	NorthStar RxLLC	OXCARBAZEPINE	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72603-272-02)
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