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
71335-2071-2	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)
68071-3944-6	68071-3944	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20260109	N/A	ANDA	ANDA078525	NuCare Pharmaceuticals, Inc.	LAMOTRIGINE	100 mg/1	60 TABLET in 1 BOTTLE (68071-3944-6)
60760-543-30	60760-543	HUMAN PRESCRIPTION DRUG	Lamotrigine	Lamotrigine	TABLET	ORAL	20220727	N/A	ANDA	ANDA078525	ST. MARY'S MEDICAL PARK PHARMACY	LAMOTRIGINE	25 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (60760-543-30)
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)
51672-4130-1	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)
51672-4130-0	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