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
63629-8490-1	63629-8490	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20180820	N/A	ANDA	ANDA205101	Bryant Ranch Prepack	GABAPENTIN	800 mg/1	100 TABLET in 1 BOTTLE (63629-8490-1)
63629-8491-1	63629-8491	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20160204	N/A	ANDA	ANDA205101	Bryant Ranch Prepack	GABAPENTIN	600 mg/1	500 TABLET in 1 BOTTLE (63629-8491-1)
63629-8492-1	63629-8492	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20180820	N/A	ANDA	ANDA205101	Bryant Ranch Prepack	GABAPENTIN	600 mg/1	100 TABLET in 1 BOTTLE (63629-8492-1)
67046-1536-3	67046-1536	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20250325	N/A	ANDA	ANDA205101	Coupler LLC	GABAPENTIN	800 mg/1	30 TABLET in 1 BLISTER PACK (67046-1536-3)
69367-134-06	69367-134	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20160411	20260201	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	20260201	ANDA	ANDA205101	Westminster Pharmaceuticals, LLC	GABAPENTIN	800 mg/1	500 TABLET in 1 BOTTLE (69367-135-06)
72162-1530-5	72162-1530	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20240202	N/A	ANDA	ANDA205101	Bryant Ranch Prepack	GABAPENTIN	600 mg/1	500 TABLET in 1 BOTTLE (72162-1530-5)
72162-1531-1	72162-1531	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20240202	N/A	ANDA	ANDA205101	Bryant Ranch Prepack	GABAPENTIN	800 mg/1	100 TABLET in 1 BOTTLE (72162-1531-1)
72162-1531-5	72162-1531	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20240202	N/A	ANDA	ANDA205101	Bryant Ranch Prepack	GABAPENTIN	800 mg/1	500 TABLET in 1 BOTTLE (72162-1531-5)
72162-1530-1	72162-1530	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20240202	N/A	ANDA	ANDA205101	Bryant Ranch Prepack	GABAPENTIN	600 mg/1	100 TABLET in 1 BOTTLE (72162-1530-1)
72789-217-60	72789-217	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20211119	N/A	ANDA	ANDA205101	PD-Rx Pharmaceuticals, Inc.	GABAPENTIN	800 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (72789-217-60)
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)
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)
76420-497-30	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)
76420-497-24	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)