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
72189-178-30	72189-178	HUMAN PRESCRIPTION DRUG	GABAPENTIN	GABAPENTIN	TABLET	ORAL	20210208	N/A	ANDA	ANDA205101	DIRECT RX	GABAPENTIN	800 mg/1	30 TABLET in 1 BOTTLE (72189-178-30)
72189-178-72	72189-178	HUMAN PRESCRIPTION DRUG	GABAPENTIN	GABAPENTIN	TABLET	ORAL	20210208	N/A	ANDA	ANDA205101	DIRECT RX	GABAPENTIN	800 mg/1	120 TABLET in 1 BOTTLE (72189-178-72)
72189-178-90	72189-178	HUMAN PRESCRIPTION DRUG	GABAPENTIN	GABAPENTIN	TABLET	ORAL	20210208	N/A	ANDA	ANDA205101	DIRECT RX	GABAPENTIN	800 mg/1	90 TABLET in 1 BOTTLE (72189-178-90)
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)
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)
71205-514-60	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)
71205-514-30	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)
71610-410-60	71610-410	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20200330	N/A	ANDA	ANDA205101	Aphena Pharma Solutions - Tennessee, LLC	GABAPENTIN	600 mg/1	90 TABLET in 1 BOTTLE (71610-410-60)
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)
50228-177-01	50228-177	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20180820	N/A	ANDA	ANDA205101	ScieGen Pharmaceuticals, Inc.	GABAPENTIN	600 mg/1	100 TABLET in 1 BOTTLE (50228-177-01)
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)