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
70518-4561-0	70518-4561	HUMAN PRESCRIPTION DRUG	Lacosamide	Lacosamide	TABLET, FILM COATED	ORAL	20260202	N/A	ANDA	ANDA214695	REMEDYREPACK INC.	LACOSAMIDE	100 mg/1	30 POUCH in 1 BOX (70518-4561-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4561-1)
60687-676-57	60687-676	HUMAN PRESCRIPTION DRUG	Lacosamide	Lacosamide	TABLET, FILM COATED	ORAL	20220601	N/A	ANDA	ANDA214695	American Health Packaging	LACOSAMIDE	50 mg/1	60 BLISTER PACK in 1 CARTON (60687-676-57) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-676-11)
60687-687-57	60687-687	HUMAN PRESCRIPTION DRUG	Lacosamide	Lacosamide	TABLET, FILM COATED	ORAL	20220601	N/A	ANDA	ANDA214695	American Health Packaging	LACOSAMIDE	100 mg/1	60 BLISTER PACK in 1 CARTON (60687-687-57) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-687-11)
60687-698-57	60687-698	HUMAN PRESCRIPTION DRUG	Lacosamide	Lacosamide	TABLET, FILM COATED	ORAL	20220603	N/A	ANDA	ANDA214695	American Health Packaging	LACOSAMIDE	200 mg/1	60 BLISTER PACK in 1 CARTON (60687-698-57) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-698-11)
80425-0510-1	80425-0510	HUMAN PRESCRIPTION DRUG	Lacosamide	Lacosamide	TABLET, FILM COATED	ORAL	20250409	N/A	ANDA	ANDA214695	Advanced Rx of Tennessee, LLC	LACOSAMIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0510-1)
80425-0510-2	80425-0510	HUMAN PRESCRIPTION DRUG	Lacosamide	Lacosamide	TABLET, FILM COATED	ORAL	20250409	N/A	ANDA	ANDA214695	Advanced Rx of Tennessee, LLC	LACOSAMIDE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0510-2)
80425-0510-3	80425-0510	HUMAN PRESCRIPTION DRUG	Lacosamide	Lacosamide	TABLET, FILM COATED	ORAL	20250409	N/A	ANDA	ANDA214695	Advanced Rx of Tennessee, LLC	LACOSAMIDE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (80425-0510-3)