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
71205-774-30	71205-774	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20230314	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	800 mg/1	30 TABLET in 1 BOTTLE (71205-774-30)
71205-774-60	71205-774	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20230314	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	800 mg/1	60 TABLET in 1 BOTTLE (71205-774-60)
71205-774-90	71205-774	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20230314	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	800 mg/1	90 TABLET in 1 BOTTLE (71205-774-90)
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)
69367-134-06	69367-134	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20160411	N/A	ANDA	ANDA205101	Westminster Pharmaceuticals, LLC	GABAPENTIN	600 mg/1	500 TABLET in 1 BOTTLE (69367-134-06)
69367-135-06	69367-135	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20160411	N/A	ANDA	ANDA205101	Westminster Pharmaceuticals, LLC	GABAPENTIN	800 mg/1	500 TABLET in 1 BOTTLE (69367-135-06)
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)
77771-177-05	77771-177	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20231103	N/A	ANDA	ANDA205101	Radha Pharmaceuticals, Inc.	GABAPENTIN	600 mg/1	500 TABLET in 1 BOTTLE (77771-177-05)
77771-177-90	77771-177	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20231103	N/A	ANDA	ANDA205101	Radha Pharmaceuticals, Inc.	GABAPENTIN	600 mg/1	90 TABLET in 1 BOTTLE (77771-177-90)
77771-178-05	77771-178	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20231103	N/A	ANDA	ANDA205101	Radha Pharmaceuticals, Inc.	GABAPENTIN	800 mg/1	500 TABLET in 1 BOTTLE (77771-178-05)
77771-178-90	77771-178	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20231103	N/A	ANDA	ANDA205101	Radha Pharmaceuticals, Inc.	GABAPENTIN	800 mg/1	90 TABLET in 1 BOTTLE (77771-178-90)
71205-931-00	71205-931	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210422	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	600 mg/1	100 TABLET in 1 BOTTLE (71205-931-00)
71205-931-30	71205-931	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210422	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	600 mg/1	30 TABLET in 1 BOTTLE (71205-931-30)
71205-931-55	71205-931	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210422	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	600 mg/1	500 TABLET in 1 BOTTLE (71205-931-55)
71205-931-60	71205-931	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210422	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	600 mg/1	60 TABLET in 1 BOTTLE (71205-931-60)
71205-931-64	71205-931	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210422	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	600 mg/1	240 TABLET in 1 BOTTLE (71205-931-64)
71205-931-67	71205-931	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210628	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	600 mg/1	270 TABLET in 1 BOTTLE (71205-931-67)
71205-931-72	71205-931	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210422	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	600 mg/1	120 TABLET in 1 BOTTLE (71205-931-72)
71205-931-76	71205-931	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210628	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	600 mg/1	360 TABLET in 1 BOTTLE (71205-931-76)
71205-931-78	71205-931	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210422	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	600 mg/1	180 TABLET in 1 BOTTLE (71205-931-78)