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
71335-1469-1	71335-1469	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200110	N/A	ANDA	ANDA200672	Bryant Ranch Prepack	LAMOTRIGINE	25 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1469-1)
0228-1435-03	0228-1435	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20160401	N/A	ANDA	ANDA200672	Actavis Pharma, Inc.	LAMOTRIGINE	50 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-1435-03)
0228-1580-03	0228-1580	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20160401	N/A	ANDA	ANDA200672	Actavis Pharma, Inc.	LAMOTRIGINE	300 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-1580-03)
0228-1638-03	0228-1638	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20160601	N/A	ANDA	ANDA200672	Actavis Pharma, Inc.	LAMOTRIGINE	250 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-1638-03)
0228-1422-03	0228-1422	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20160401	N/A	ANDA	ANDA200672	Actavis Pharma, Inc.	LAMOTRIGINE	100 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-1422-03)
0228-1410-03	0228-1410	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20160401	N/A	ANDA	ANDA200672	Actavis Pharma, Inc.	LAMOTRIGINE	25 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-1410-03)
0228-1453-03	0228-1453	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20160401	N/A	ANDA	ANDA200672	Actavis Pharma, Inc.	LAMOTRIGINE	200 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-1453-03)