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
77771-178-05	77771-178	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20231103	N/A	ANDA	ANDA205101	Radha Pharmaceuticals, Inc.	GABAPENTIN	800 mg/1	500 TABLET in 1 BOTTLE (77771-178-05)
77771-178-90	77771-178	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20231103	N/A	ANDA	ANDA205101	Radha Pharmaceuticals, Inc.	GABAPENTIN	800 mg/1	90 TABLET in 1 BOTTLE (77771-178-90)
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)
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)