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
50090-7080-0	50090-7080	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20240201	N/A	ANDA	ANDA217116	A-S Medication Solutions	GABAPENTIN	600 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-7080-0)
50090-7080-1	50090-7080	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20240201	N/A	ANDA	ANDA217116	A-S Medication Solutions	GABAPENTIN	600 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (50090-7080-1)
50090-7080-2	50090-7080	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20240201	N/A	ANDA	ANDA217116	A-S Medication Solutions	GABAPENTIN	600 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-7080-2)
50090-7081-0	50090-7081	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20240201	N/A	ANDA	ANDA217116	A-S Medication Solutions	GABAPENTIN	600 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-7081-0)
70010-227-01	70010-227	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20230627	N/A	ANDA	ANDA217116	Granules Pharmaceuticals Inc.	GABAPENTIN	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70010-227-01)
70010-227-05	70010-227	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20230627	N/A	ANDA	ANDA217116	Granules Pharmaceuticals Inc.	GABAPENTIN	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (70010-227-05)
70010-228-05	70010-228	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20230627	N/A	ANDA	ANDA217116	Granules Pharmaceuticals Inc.	GABAPENTIN	800 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (70010-228-05)
70010-228-01	70010-228	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20230627	N/A	ANDA	ANDA217116	Granules Pharmaceuticals Inc.	GABAPENTIN	800 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70010-228-01)