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
0228-2637-50	0228-2637	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20041004	20250731	ANDA	ANDA075694	Actavis Pharma, Inc.	GABAPENTIN	800 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (0228-2637-50)
0228-2637-11	0228-2637	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20041004	20250731	ANDA	ANDA075694	Actavis Pharma, Inc.	GABAPENTIN	800 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0228-2637-11)
0228-2636-50	0228-2636	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20041214	20250531	ANDA	ANDA075694	Actavis Pharma, Inc.	GABAPENTIN	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (0228-2636-50)
0228-2636-11	0228-2636	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20041214	20250531	ANDA	ANDA075694	Actavis Pharma, Inc.	GABAPENTIN	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0228-2636-11)
63187-006-90	63187-006	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20140501	N/A	ANDA	ANDA075694	Proficient Rx	GABAPENTIN	600 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63187-006-90)