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
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)
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)
71205-932-76	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)
71205-932-90	71205-932	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210422	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	800 mg/1	90 TABLET in 1 BOTTLE (71205-932-90)
50228-178-01	50228-178	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20180820	N/A	ANDA	ANDA205101	ScieGen Pharmaceuticals, Inc.	GABAPENTIN	800 mg/1	100 TABLET in 1 BOTTLE (50228-178-01)
50228-178-05	50228-178	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20160204	N/A	ANDA	ANDA205101	ScieGen Pharmaceuticals, Inc.	GABAPENTIN	800 mg/1	500 TABLET in 1 BOTTLE (50228-178-05)
50228-178-30	50228-178	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20160204	N/A	ANDA	ANDA205101	ScieGen Pharmaceuticals, Inc.	GABAPENTIN	800 mg/1	30 TABLET in 1 BOTTLE (50228-178-30)
68071-2206-1	68071-2206	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20200706	N/A	ANDA	ANDA205101	NuCare Pharmaceuticals,Inc.	GABAPENTIN	800 mg/1	100 TABLET in 1 BOTTLE (68071-2206-1)
68071-2214-9	68071-2214	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20200708	N/A	ANDA	ANDA205101	NuCare Pharmaceuticals,Inc.	GABAPENTIN	800 mg/1	90 TABLET in 1 BOTTLE (68071-2214-9)
68788-7840-1	68788-7840	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210118	N/A	ANDA	ANDA205101	Preferred Pharmaceuticals, Inc.	GABAPENTIN	600 mg/1	100 TABLET in 1 BOTTLE (68788-7840-1)
68788-7840-3	68788-7840	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210118	N/A	ANDA	ANDA205101	Preferred Pharmaceuticals, Inc.	GABAPENTIN	600 mg/1	30 TABLET in 1 BOTTLE (68788-7840-3)
68788-7840-6	68788-7840	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210118	N/A	ANDA	ANDA205101	Preferred Pharmaceuticals, Inc.	GABAPENTIN	600 mg/1	60 TABLET in 1 BOTTLE (68788-7840-6)
68788-7840-8	68788-7840	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210118	N/A	ANDA	ANDA205101	Preferred Pharmaceuticals, Inc.	GABAPENTIN	600 mg/1	120 TABLET in 1 BOTTLE (68788-7840-8)
68788-7840-9	68788-7840	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210118	N/A	ANDA	ANDA205101	Preferred Pharmaceuticals, Inc.	GABAPENTIN	600 mg/1	90 TABLET in 1 BOTTLE (68788-7840-9)
68788-7847-1	68788-7847	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210121	N/A	ANDA	ANDA205101	Preferred Pharmaceuticals Inc.	GABAPENTIN	600 mg/1	100 TABLET in 1 BOTTLE (68788-7847-1)
68788-7847-3	68788-7847	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210121	N/A	ANDA	ANDA205101	Preferred Pharmaceuticals Inc.	GABAPENTIN	600 mg/1	30 TABLET in 1 BOTTLE (68788-7847-3)