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
51672-4130-1	51672-4130	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20090127	N/A	ANDA	ANDA078525	Sun Pharmaceutical Industries, Inc.	LAMOTRIGINE	25 mg/1	100 TABLET in 1 BOTTLE (51672-4130-1)
51672-4130-3	51672-4130	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20090127	N/A	ANDA	ANDA078525	Sun Pharmaceutical Industries, Inc.	LAMOTRIGINE	25 mg/1	1000 TABLET in 1 BOTTLE (51672-4130-3)
51672-4130-4	51672-4130	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20090127	N/A	ANDA	ANDA078525	Sun Pharmaceutical Industries, Inc.	LAMOTRIGINE	25 mg/1	60 TABLET in 1 BOTTLE (51672-4130-4)
51672-4130-6	51672-4130	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20090127	N/A	ANDA	ANDA078525	Sun Pharmaceutical Industries, Inc.	LAMOTRIGINE	25 mg/1	30 TABLET in 1 BOTTLE (51672-4130-6)
51672-4131-0	51672-4131	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20090127	N/A	ANDA	ANDA078525	Sun Pharmaceutical Industries, Inc.	LAMOTRIGINE	100 mg/1	10 BLISTER PACK in 1 CARTON (51672-4131-0) / 10 TABLET in 1 BLISTER PACK
51672-4131-1	51672-4131	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20090127	N/A	ANDA	ANDA078525	Sun Pharmaceutical Industries, Inc.	LAMOTRIGINE	100 mg/1	100 TABLET in 1 BOTTLE (51672-4131-1)
51672-4131-3	51672-4131	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20090127	N/A	ANDA	ANDA078525	Sun Pharmaceutical Industries, Inc.	LAMOTRIGINE	100 mg/1	1000 TABLET in 1 BOTTLE (51672-4131-3)
51672-4131-4	51672-4131	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20090127	N/A	ANDA	ANDA078525	Sun Pharmaceutical Industries, Inc.	LAMOTRIGINE	100 mg/1	60 TABLET in 1 BOTTLE (51672-4131-4)
51672-4131-6	51672-4131	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20090127	N/A	ANDA	ANDA078525	Sun Pharmaceutical Industries, Inc.	LAMOTRIGINE	100 mg/1	30 TABLET in 1 BOTTLE (51672-4131-6)