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
71610-767-45	71610-767	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20240109	N/A	ANDA	ANDA205101	Aphena Pharma Solutions - Tennessee, LLC	GABAPENTIN	600 mg/1	45 TABLET in 1 BOTTLE (71610-767-45)
71610-767-60	71610-767	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20240109	N/A	ANDA	ANDA205101	Aphena Pharma Solutions - Tennessee, LLC	GABAPENTIN	600 mg/1	90 TABLET in 1 BOTTLE (71610-767-60)
71205-932-00	71205-932	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210422	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	800 mg/1	100 TABLET in 1 BOTTLE (71205-932-00)
71205-932-64	71205-932	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210422	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	800 mg/1	240 TABLET in 1 BOTTLE (71205-932-64)
71205-932-67	71205-932	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210628	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	800 mg/1	270 TABLET in 1 BOTTLE (71205-932-67)
71205-932-72	71205-932	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210422	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	800 mg/1	120 TABLET in 1 BOTTLE (71205-932-72)
71205-932-30	71205-932	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210422	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	800 mg/1	30 TABLET in 1 BOTTLE (71205-932-30)
71205-932-55	71205-932	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210422	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	800 mg/1	500 TABLET in 1 BOTTLE (71205-932-55)
71205-932-60	71205-932	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210422	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	800 mg/1	60 TABLET in 1 BOTTLE (71205-932-60)
72162-1530-1	72162-1530	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20180820	N/A	ANDA	ANDA205101	Bryant Ranch Prepack	GABAPENTIN	600 mg/1	100 TABLET in 1 BOTTLE (72162-1530-1)
72162-1530-5	72162-1530	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20180820	N/A	ANDA	ANDA205101	Bryant Ranch Prepack	GABAPENTIN	600 mg/1	500 TABLET in 1 BOTTLE (72162-1530-5)
72162-1531-1	72162-1531	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20180820	N/A	ANDA	ANDA205101	Bryant Ranch Prepack	GABAPENTIN	800 mg/1	100 TABLET in 1 BOTTLE (72162-1531-1)
72162-1531-5	72162-1531	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20180820	N/A	ANDA	ANDA205101	Bryant Ranch Prepack	GABAPENTIN	800 mg/1	500 TABLET in 1 BOTTLE (72162-1531-5)
76420-235-12	76420-235	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20220707	N/A	ANDA	ANDA205101	Asclemed USA, Inc.	GABAPENTIN	600 mg/1	120 TABLET in 1 BOTTLE (76420-235-12)
76420-235-24	76420-235	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20220707	N/A	ANDA	ANDA205101	Asclemed USA, Inc.	GABAPENTIN	600 mg/1	240 TABLET in 1 BOTTLE (76420-235-24)
76420-235-30	76420-235	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20220707	N/A	ANDA	ANDA205101	Asclemed USA, Inc.	GABAPENTIN	600 mg/1	30 TABLET in 1 BOTTLE (76420-235-30)
76420-235-60	76420-235	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20220707	N/A	ANDA	ANDA205101	Asclemed USA, Inc.	GABAPENTIN	600 mg/1	60 TABLET in 1 BOTTLE (76420-235-60)
76420-235-90	76420-235	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20220707	N/A	ANDA	ANDA205101	Asclemed USA, Inc.	GABAPENTIN	600 mg/1	90 TABLET in 1 BOTTLE (76420-235-90)
71205-932-76	71205-932	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210628	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	800 mg/1	360 TABLET in 1 BOTTLE (71205-932-76)
71205-932-78	71205-932	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210422	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	800 mg/1	180 TABLET in 1 BOTTLE (71205-932-78)