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
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)
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)
70518-4532-0	70518-4532	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20251207	N/A	ANDA	ANDA217116	REMEDYREPACK INC.	GABAPENTIN	600 mg/1	100 POUCH in 1 BOX (70518-4532-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4532-1)
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)
70010-227-01	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)