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
51672-4133-0	51672-4133	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20090127	N/A	ANDA	ANDA078525	Sun Pharmaceutical Industries, Inc.	LAMOTRIGINE	200 mg/1	10 BLISTER PACK in 1 CARTON (51672-4133-0) / 10 TABLET in 1 BLISTER PACK
51672-4133-1	51672-4133	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20090127	N/A	ANDA	ANDA078525	Sun Pharmaceutical Industries, Inc.	LAMOTRIGINE	200 mg/1	100 TABLET in 1 BOTTLE (51672-4133-1)
51672-4133-2	51672-4133	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20221025	N/A	ANDA	ANDA078525	Sun Pharmaceutical Industries, Inc.	LAMOTRIGINE	200 mg/1	500 TABLET in 1 BOTTLE (51672-4133-2)
51672-4133-3	51672-4133	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20090127	N/A	ANDA	ANDA078525	Sun Pharmaceutical Industries, Inc.	LAMOTRIGINE	200 mg/1	1000 TABLET in 1 BOTTLE (51672-4133-3)
51672-4133-4	51672-4133	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20090127	N/A	ANDA	ANDA078525	Sun Pharmaceutical Industries, Inc.	LAMOTRIGINE	200 mg/1	60 TABLET in 1 BOTTLE (51672-4133-4)
51672-4133-6	51672-4133	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20090127	N/A	ANDA	ANDA078525	Sun Pharmaceutical Industries, Inc.	LAMOTRIGINE	200 mg/1	30 TABLET in 1 BOTTLE (51672-4133-6)
71335-2071-1	71335-2071	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20240403	N/A	ANDA	ANDA078525	Bryant Ranch Prepack	LAMOTRIGINE	150 mg/1	60 TABLET in 1 BOTTLE (71335-2071-1)
71335-2071-2	71335-2071	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20220325	N/A	ANDA	ANDA078525	Bryant Ranch Prepack	LAMOTRIGINE	150 mg/1	30 TABLET in 1 BOTTLE (71335-2071-2)
71335-2071-3	71335-2071	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20240403	N/A	ANDA	ANDA078525	Bryant Ranch Prepack	LAMOTRIGINE	150 mg/1	90 TABLET in 1 BOTTLE (71335-2071-3)
71335-2071-4	71335-2071	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20240403	N/A	ANDA	ANDA078525	Bryant Ranch Prepack	LAMOTRIGINE	150 mg/1	120 TABLET in 1 BOTTLE (71335-2071-4)
71335-2071-5	71335-2071	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20240403	N/A	ANDA	ANDA078525	Bryant Ranch Prepack	LAMOTRIGINE	150 mg/1	180 TABLET in 1 BOTTLE (71335-2071-5)
51672-4132-0	51672-4132	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20090127	N/A	ANDA	ANDA078525	Sun Pharmaceutical Industries, Inc.	LAMOTRIGINE	150 mg/1	10 BLISTER PACK in 1 CARTON (51672-4132-0) / 10 TABLET in 1 BLISTER PACK
51672-4132-1	51672-4132	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20090127	N/A	ANDA	ANDA078525	Sun Pharmaceutical Industries, Inc.	LAMOTRIGINE	150 mg/1	100 TABLET in 1 BOTTLE (51672-4132-1)
51672-4132-2	51672-4132	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20221025	N/A	ANDA	ANDA078525	Sun Pharmaceutical Industries, Inc.	LAMOTRIGINE	150 mg/1	500 TABLET in 1 BOTTLE (51672-4132-2)
51672-4132-3	51672-4132	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20090127	N/A	ANDA	ANDA078525	Sun Pharmaceutical Industries, Inc.	LAMOTRIGINE	150 mg/1	1000 TABLET in 1 BOTTLE (51672-4132-3)
51672-4132-4	51672-4132	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20090127	N/A	ANDA	ANDA078525	Sun Pharmaceutical Industries, Inc.	LAMOTRIGINE	150 mg/1	60 TABLET in 1 BOTTLE (51672-4132-4)
51672-4132-6	51672-4132	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20090127	N/A	ANDA	ANDA078525	Sun Pharmaceutical Industries, Inc.	LAMOTRIGINE	150 mg/1	30 TABLET in 1 BOTTLE (51672-4132-6)
51672-4130-0	51672-4130	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20090127	N/A	ANDA	ANDA078525	Sun Pharmaceutical Industries, Inc.	LAMOTRIGINE	25 mg/1	10 BLISTER PACK in 1 CARTON (51672-4130-0) / 10 TABLET in 1 BLISTER PACK
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)