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
76420-235-30	76420-235	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20220707	N/A	ANDA	ANDA205101	Asclemed USA, Inc.	GABAPENTIN	600 mg/1	30 TABLET in 1 BOTTLE (76420-235-30)
76420-235-60	76420-235	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20220707	N/A	ANDA	ANDA205101	Asclemed USA, Inc.	GABAPENTIN	600 mg/1	60 TABLET in 1 BOTTLE (76420-235-60)
76420-235-90	76420-235	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20220707	N/A	ANDA	ANDA205101	Asclemed USA, Inc.	GABAPENTIN	600 mg/1	90 TABLET in 1 BOTTLE (76420-235-90)
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)
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)
76420-497-12	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)
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)
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)
50228-177-05	50228-177	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20160204	N/A	ANDA	ANDA205101	ScieGen Pharmaceuticals, Inc.	GABAPENTIN	600 mg/1	500 TABLET in 1 BOTTLE (50228-177-05)
50228-177-30	50228-177	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20160204	N/A	ANDA	ANDA205101	ScieGen Pharmaceuticals, Inc.	GABAPENTIN	600 mg/1	30 TABLET in 1 BOTTLE (50228-177-30)
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)
82619-145-01	82619-145	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20240901	N/A	ANDA	ANDA205101	Creekwood Pharmaceuticals LLC	GABAPENTIN	600 mg/1	100 TABLET in 1 BOTTLE (82619-145-01)
82619-145-02	82619-145	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20240901	N/A	ANDA	ANDA205101	Creekwood Pharmaceuticals LLC	GABAPENTIN	600 mg/1	500 TABLET in 1 BOTTLE (82619-145-02)
82619-146-01	82619-146	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20240901	N/A	ANDA	ANDA205101	Creekwood Pharmaceuticals LLC	GABAPENTIN	800 mg/1	100 TABLET in 1 BOTTLE (82619-146-01)
82619-146-02	82619-146	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20240901	N/A	ANDA	ANDA205101	Creekwood Pharmaceuticals LLC	GABAPENTIN	800 mg/1	500 TABLET in 1 BOTTLE (82619-146-02)