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
71610-069-45	71610-069	HUMAN PRESCRIPTION DRUG	gabapentin	gabapentin	TABLET, FILM COATED	ORAL	20210226	N/A	ANDA	ANDA077525	Aphena Pharma Solutions - Tennessee, LLC	GABAPENTIN	600 mg/1	45 TABLET, FILM COATED in 1 BOTTLE (71610-069-45)
71610-069-60	71610-069	HUMAN PRESCRIPTION DRUG	gabapentin	gabapentin	TABLET, FILM COATED	ORAL	20180515	N/A	ANDA	ANDA077525	Aphena Pharma Solutions - Tennessee, LLC	GABAPENTIN	600 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71610-069-60)
71610-069-80	71610-069	HUMAN PRESCRIPTION DRUG	gabapentin	gabapentin	TABLET, FILM COATED	ORAL	20180515	N/A	ANDA	ANDA077525	Aphena Pharma Solutions - Tennessee, LLC	GABAPENTIN	600 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71610-069-80)
71610-069-92	71610-069	HUMAN PRESCRIPTION DRUG	gabapentin	gabapentin	TABLET, FILM COATED	ORAL	20180515	N/A	ANDA	ANDA077525	Aphena Pharma Solutions - Tennessee, LLC	GABAPENTIN	600 mg/1	270 TABLET, FILM COATED in 1 BOTTLE (71610-069-92)
62756-204-01	62756-204	HUMAN PRESCRIPTION DRUG	gabapentin	gabapentin	TABLET, FILM COATED	ORAL	20220901	N/A	ANDA	ANDA077525	Sun Pharmaceutical Industries, Inc.	GABAPENTIN	800 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (62756-204-01)
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)
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)