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
62756-204-03	62756-204	HUMAN PRESCRIPTION DRUG	gabapentin	gabapentin	TABLET, FILM COATED	ORAL	20220901	N/A	ANDA	ANDA077525	Sun Pharmaceutical Industries, Inc.	GABAPENTIN	800 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (62756-204-03)
71335-1018-2	71335-1018	HUMAN PRESCRIPTION DRUG	gabapentin	gabapentin	TABLET, FILM COATED	ORAL	20100226	N/A	ANDA	ANDA077525	Bryant Ranch Prepack	GABAPENTIN	800 mg/1	18 TABLET, FILM COATED in 1 BOTTLE (71335-1018-2)
62756-202-01	62756-202	HUMAN PRESCRIPTION DRUG	gabapentin	gabapentin	TABLET, FILM COATED	ORAL	20220901	N/A	ANDA	ANDA077525	Sun Pharmaceutical Industries, Inc.	GABAPENTIN	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (62756-202-01)
62756-202-03	62756-202	HUMAN PRESCRIPTION DRUG	gabapentin	gabapentin	TABLET, FILM COATED	ORAL	20220901	N/A	ANDA	ANDA077525	Sun Pharmaceutical Industries, Inc.	GABAPENTIN	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (62756-202-03)