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
68788-7757-9	68788-7757	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20200701	N/A	ANDA	ANDA205101	Preferred Pharmaceuticals, Inc.	GABAPENTIN	800 mg/1	90 TABLET in 1 BOTTLE (68788-7757-9)
68788-7774-1	68788-7774	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20200824	N/A	ANDA	ANDA205101	Preferred Pharmaceuticals, Inc.	GABAPENTIN	800 mg/1	100 TABLET in 1 BOTTLE (68788-7774-1)
68788-7774-3	68788-7774	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20200824	N/A	ANDA	ANDA205101	Preferred Pharmaceuticals, Inc.	GABAPENTIN	800 mg/1	30 TABLET in 1 BOTTLE (68788-7774-3)
68788-7774-6	68788-7774	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20200824	N/A	ANDA	ANDA205101	Preferred Pharmaceuticals, Inc.	GABAPENTIN	800 mg/1	60 TABLET in 1 BOTTLE (68788-7774-6)
68788-7774-8	68788-7774	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20200824	N/A	ANDA	ANDA205101	Preferred Pharmaceuticals, Inc.	GABAPENTIN	800 mg/1	120 TABLET in 1 BOTTLE (68788-7774-8)
68788-7774-9	68788-7774	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20200824	N/A	ANDA	ANDA205101	Preferred Pharmaceuticals, Inc.	GABAPENTIN	800 mg/1	90 TABLET in 1 BOTTLE (68788-7774-9)
71205-514-30	71205-514	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20201209	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	800 mg/1	30 TABLET in 1 BOTTLE (71205-514-30)
71205-514-60	71205-514	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20201209	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	800 mg/1	60 TABLET in 1 BOTTLE (71205-514-60)
71205-514-90	71205-514	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20201209	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	800 mg/1	90 TABLET in 1 BOTTLE (71205-514-90)
71205-533-30	71205-533	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210209	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	600 mg/1	30 TABLET in 1 BOTTLE (71205-533-30)
71205-533-60	71205-533	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210209	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	600 mg/1	60 TABLET in 1 BOTTLE (71205-533-60)
71205-533-90	71205-533	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20210209	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	600 mg/1	90 TABLET in 1 BOTTLE (71205-533-90)
72189-313-60	72189-313	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20220117	N/A	ANDA	ANDA205101	Directrx	GABAPENTIN	600 mg/1	60 TABLET in 1 BOTTLE (72189-313-60)
72189-313-72	72189-313	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20220117	N/A	ANDA	ANDA205101	Directrx	GABAPENTIN	600 mg/1	120 TABLET in 1 BOTTLE (72189-313-72)
72189-313-90	72189-313	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20220117	N/A	ANDA	ANDA205101	Directrx	GABAPENTIN	600 mg/1	90 TABLET in 1 BOTTLE (72189-313-90)
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)