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
60290-067-01	60290-067	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20260101	N/A	ANDA	ANDA218341	Umedica Laboratories USA Inc.	OXCARBAZEPINE	150 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (60290-067-01)
60290-067-02	60290-067	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20260101	N/A	ANDA	ANDA218341	Umedica Laboratories USA Inc.	OXCARBAZEPINE	150 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (60290-067-02)
60290-069-01	60290-069	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20260101	N/A	ANDA	ANDA218341	Umedica Laboratories USA Inc.	OXCARBAZEPINE	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (60290-069-01)
60290-069-02	60290-069	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20260101	N/A	ANDA	ANDA218341	Umedica Laboratories USA Inc.	OXCARBAZEPINE	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (60290-069-02)
60290-068-01	60290-068	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20260101	N/A	ANDA	ANDA218341	Umedica Laboratories USA Inc.	OXCARBAZEPINE	300 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (60290-068-01)
60290-068-02	60290-068	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20260101	N/A	ANDA	ANDA218341	Umedica Laboratories USA Inc.	OXCARBAZEPINE	300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (60290-068-02)