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
67877-428-05	67877-428	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20151101	N/A	ANDA	ANDA206402	Ascend Laboratories, LLC	GABAPENTIN	600 mg/1	500 TABLET in 1 BOTTLE (67877-428-05)
67877-428-10	67877-428	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20151101	N/A	ANDA	ANDA206402	Ascend Laboratories, LLC	GABAPENTIN	600 mg/1	1000 TABLET in 1 BOTTLE (67877-428-10)
67877-428-38	67877-428	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20151101	N/A	ANDA	ANDA206402	Ascend Laboratories, LLC	GABAPENTIN	600 mg/1	100 BLISTER PACK in 1 CARTON (67877-428-38) / 10 TABLET in 1 BLISTER PACK
67877-429-01	67877-429	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20151101	N/A	ANDA	ANDA206402	Ascend Laboratories, LLC	GABAPENTIN	800 mg/1	100 TABLET in 1 BOTTLE (67877-429-01)
67877-429-05	67877-429	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20151101	N/A	ANDA	ANDA206402	Ascend Laboratories, LLC	GABAPENTIN	800 mg/1	500 TABLET in 1 BOTTLE (67877-429-05)
67877-429-10	67877-429	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20151101	N/A	ANDA	ANDA206402	Ascend Laboratories, LLC	GABAPENTIN	800 mg/1	1000 TABLET in 1 BOTTLE (67877-429-10)
67877-429-38	67877-429	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20151101	N/A	ANDA	ANDA206402	Ascend Laboratories, LLC	GABAPENTIN	800 mg/1	100 BLISTER PACK in 1 CARTON (67877-429-38) / 10 TABLET in 1 BLISTER PACK