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
76420-497-24	76420-497	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20221010	N/A	ANDA	ANDA205101	Asclemed USA, Inc.	GABAPENTIN	800 mg/1	240 TABLET in 1 BOTTLE (76420-497-24)
76420-497-30	76420-497	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20221010	N/A	ANDA	ANDA205101	Asclemed USA, Inc.	GABAPENTIN	800 mg/1	30 TABLET in 1 BOTTLE (76420-497-30)
76420-497-60	76420-497	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20221010	N/A	ANDA	ANDA205101	Asclemed USA, Inc.	GABAPENTIN	800 mg/1	60 TABLET in 1 BOTTLE (76420-497-60)
76420-497-90	76420-497	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20221010	N/A	ANDA	ANDA205101	Asclemed USA, Inc.	GABAPENTIN	800 mg/1	90 TABLET in 1 BOTTLE (76420-497-90)
76420-497-12	76420-497	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20221010	N/A	ANDA	ANDA205101	Asclemed USA, Inc.	GABAPENTIN	800 mg/1	120 TABLET in 1 BOTTLE (76420-497-12)
76420-497-05	76420-497	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20221010	N/A	ANDA	ANDA205101	Asclemed USA, Inc.	GABAPENTIN	800 mg/1	500 TABLET in 1 BOTTLE (76420-497-05)
76420-497-01	76420-497	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20221010	N/A	ANDA	ANDA205101	Asclemed USA, Inc.	GABAPENTIN	800 mg/1	100 TABLET in 1 BOTTLE (76420-497-01)
82804-015-30	82804-015	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20231003	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	600 mg/1	30 TABLET in 1 BOTTLE (82804-015-30)
82804-015-60	82804-015	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20231003	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	600 mg/1	60 TABLET in 1 BOTTLE (82804-015-60)
82804-015-90	82804-015	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20231003	N/A	ANDA	ANDA205101	Proficient Rx LP	GABAPENTIN	600 mg/1	90 TABLET in 1 BOTTLE (82804-015-90)
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)
71205-514-90	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)
71205-514-30	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)
71205-533-60	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)
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)
71610-737-45	71610-737	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20230922	N/A	ANDA	ANDA205101	Aphena Pharma Solutions - Tennessee, LLC	GABAPENTIN	800 mg/1	45 TABLET in 1 BOTTLE (71610-737-45)
71610-737-70	71610-737	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20230922	N/A	ANDA	ANDA205101	Aphena Pharma Solutions - Tennessee, LLC	GABAPENTIN	800 mg/1	120 TABLET in 1 BOTTLE (71610-737-70)
71610-737-73	71610-737	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20230922	N/A	ANDA	ANDA205101	Aphena Pharma Solutions - Tennessee, LLC	GABAPENTIN	800 mg/1	135 TABLET in 1 BOTTLE (71610-737-73)
71610-737-80	71610-737	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20230922	N/A	ANDA	ANDA205101	Aphena Pharma Solutions - Tennessee, LLC	GABAPENTIN	800 mg/1	180 TABLET in 1 BOTTLE (71610-737-80)