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
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)
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)
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)
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)
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)