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
16714-625-01	16714-625	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET, EXTENDED RELEASE	ORAL	20170620	N/A	ANDA	ANDA202383	NorthStar Rx LLC	LAMOTRIGINE	100 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-625-01)
16714-626-01	16714-626	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET, EXTENDED RELEASE	ORAL	20170620	N/A	ANDA	ANDA202383	NorthStar Rx LLC	LAMOTRIGINE	200 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-626-01)
16714-627-01	16714-627	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET, EXTENDED RELEASE	ORAL	20170620	N/A	ANDA	ANDA202383	NorthStar Rx LLC	LAMOTRIGINE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-627-01)
68788-6868-3	68788-6868	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET, EXTENDED RELEASE	ORAL	20170111	N/A	ANDA	ANDA202383	Preferred Pharmaceuticals Inc.	LAMOTRIGINE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-6868-3)
68788-6868-6	68788-6868	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET, EXTENDED RELEASE	ORAL	20170111	N/A	ANDA	ANDA202383	Preferred Pharmaceuticals Inc.	LAMOTRIGINE	300 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-6868-6)
16714-623-01	16714-623	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET, EXTENDED RELEASE	ORAL	20170620	N/A	ANDA	ANDA202383	NorthStar Rx LLC	LAMOTRIGINE	25 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-623-01)
16714-893-01	16714-893	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET, EXTENDED RELEASE	ORAL	20181120	N/A	ANDA	ANDA202383	NorthStar Rx LLC	LAMOTRIGINE	250 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-893-01)