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
37835-594-03	37835-594	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20250301	N/A	ANDA	ANDA091353	Bi-Mart	NAPROXEN SODIUM	220 mg/1	300 TABLET in 1 BOTTLE (37835-594-03)
21130-061-05	21130-061	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20230930	N/A	ANDA	ANDA091353	Safeway, Inc	NAPROXEN SODIUM	220 mg/1	50 TABLET in 1 BOTTLE (21130-061-05)
21130-061-09	21130-061	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20230930	N/A	ANDA	ANDA091353	Safeway, Inc	NAPROXEN SODIUM	220 mg/1	90 TABLET in 1 BOTTLE (21130-061-09)
21130-062-05	21130-062	HUMAN OTC DRUG	Naproxen	Naproxen	TABLET	ORAL	20230830	N/A	ANDA	ANDA091353	Safeway, Inc	NAPROXEN SODIUM	220 mg/1	50 TABLET in 1 BOTTLE (21130-062-05)
21130-062-09	21130-062	HUMAN OTC DRUG	Naproxen	Naproxen	TABLET	ORAL	20230830	N/A	ANDA	ANDA091353	Safeway, Inc	NAPROXEN SODIUM	220 mg/1	90 TABLET in 1 BOTTLE (21130-062-09)
21130-062-20	21130-062	HUMAN OTC DRUG	Naproxen	Naproxen	TABLET	ORAL	20230930	N/A	ANDA	ANDA091353	Safeway, Inc	NAPROXEN SODIUM	220 mg/1	200 TABLET in 1 BOTTLE (21130-062-20)
82501-1576-1	82501-1576	HUMAN OTC DRUG	Pain Relief	Naproxen Sodium	TABLET, FILM COATED	ORAL	20220530	N/A	ANDA	ANDA091353	Gobrands, Inc	NAPROXEN SODIUM	220 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (82501-1576-1)
69848-010-01	69848-010	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20190701	N/A	ANDA	ANDA091353	Granules USA, Inc.	NAPROXEN SODIUM	220 mg/1	10 TABLET in 1 BOTTLE (69848-010-01)
69848-010-05	69848-010	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20230301	N/A	ANDA	ANDA091353	Granules USA, Inc.	NAPROXEN SODIUM	220 mg/1	50 TABLET in 1 BOTTLE (69848-010-05)
69848-010-10	69848-010	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20230301	N/A	ANDA	ANDA091353	Granules USA, Inc.	NAPROXEN SODIUM	220 mg/1	100 TABLET in 1 BOTTLE (69848-010-10)
69517-109-02	69517-109	HUMAN OTC DRUG	All Day Pain Relief	Naproxen Sodium Tablets, 220 mg	TABLET	ORAL	20160407	N/A	ANDA	ANDA091353	HealthLife of USA LLC	NAPROXEN SODIUM	220 mg/1	2 POUCH in 1 POUCH (69517-109-02) / 2 TABLET in 1 POUCH
69517-109-04	69517-109	HUMAN OTC DRUG	All Day Pain Relief	Naproxen Sodium Tablets, 220 mg	TABLET	ORAL	20160407	N/A	ANDA	ANDA091353	HealthLife of USA LLC	NAPROXEN SODIUM	220 mg/1	400 BOTTLE in 1 BOTTLE (69517-109-04) / 100 BOTTLE in 1 BOTTLE (69517-109-01) / 24 CARTON in 1 BOTTLE (69517-109-24) / 1 TABLET in 1 CARTON
69517-109-25	69517-109	HUMAN OTC DRUG	All Day Pain Relief	Naproxen Sodium Tablets, 220 mg	TABLET	ORAL	20160407	N/A	ANDA	ANDA091353	HealthLife of USA LLC	NAPROXEN SODIUM	220 mg/1	25 POUCH in 1 BOX (69517-109-25) / 2 TABLET in 1 POUCH
69517-109-50	69517-109	HUMAN OTC DRUG	All Day Pain Relief	Naproxen Sodium Tablets, 220 mg	TABLET	ORAL	20160407	N/A	ANDA	ANDA091353	HealthLife of USA LLC	NAPROXEN SODIUM	220 mg/1	50 POUCH in 1 BOX (69517-109-50) / 2 TABLET in 1 POUCH