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
71335-2819-2	71335-2819	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20251022	N/A	ANDA	ANDA200651	Bryant Ranch Prepack	GABAPENTIN	800 mg/1	18 TABLET, FILM COATED in 1 BOTTLE (71335-2819-2)
71335-2819-3	71335-2819	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20251022	N/A	ANDA	ANDA200651	Bryant Ranch Prepack	GABAPENTIN	800 mg/1	58 TABLET, FILM COATED in 1 BOTTLE (71335-2819-3)
71335-2819-4	71335-2819	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20251022	N/A	ANDA	ANDA200651	Bryant Ranch Prepack	GABAPENTIN	800 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-2819-4)
71335-2819-5	71335-2819	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20251022	N/A	ANDA	ANDA200651	Bryant Ranch Prepack	GABAPENTIN	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2819-5)
71335-2819-6	71335-2819	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20251022	N/A	ANDA	ANDA200651	Bryant Ranch Prepack	GABAPENTIN	800 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-2819-6)
16714-330-01	16714-330	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20111006	N/A	ANDA	ANDA200651	NorthStar Rx LLC	GABAPENTIN	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16714-330-01)
16714-330-02	16714-330	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20111006	N/A	ANDA	ANDA200651	NorthStar Rx LLC	GABAPENTIN	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (16714-330-02)
16714-332-01	16714-332	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20111006	N/A	ANDA	ANDA200651	NorthStar Rx LLC	GABAPENTIN	800 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16714-332-01)
16714-332-02	16714-332	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20111006	N/A	ANDA	ANDA200651	NorthStar Rx LLC	GABAPENTIN	800 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (16714-332-02)
72189-092-90	72189-092	HUMAN PRESCRIPTION DRUG	GABAPENTIN	GABAPENTIN	TABLET, FILM COATED	ORAL	20200515	N/A	ANDA	ANDA200651	DIRECT RX	GABAPENTIN	800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72189-092-90)
63187-148-90	63187-148	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20190101	N/A	ANDA	ANDA200651	Proficient Rx LP	GABAPENTIN	800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63187-148-90)