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
72865-284-05	72865-284	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20240718	N/A	ANDA	ANDA215939	XLCare Pharmaceuticals Inc.	OXCARBAZEPINE	300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72865-284-05)
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)