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
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
62207-327-42	62207-327	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20210716	N/A	ANDA	ANDA091353	Granules India Ltd	NAPROXEN SODIUM	220 mg/1	50 TABLET in 1 BOTTLE (62207-327-42)
69729-123-12	69729-123	HUMAN OTC DRUG	PROXEN NP 660	Naproxen Sodium	TABLET	ORAL	20231107	N/A	ANDA	ANDA091353	OPMX LLC	NAPROXEN SODIUM	220 mg/1	1 BLISTER PACK in 1 CARTON (69729-123-12) / 12 TABLET in 1 BLISTER PACK
69729-123-24	69729-123	HUMAN OTC DRUG	PROXEN NP 660	Naproxen Sodium	TABLET	ORAL	20231116	N/A	ANDA	ANDA091353	OPMX LLC	NAPROXEN SODIUM	220 mg/1	2 BLISTER PACK in 1 CARTON (69729-123-24) / 12 TABLET in 1 BLISTER PACK
69729-123-50	69729-123	HUMAN OTC DRUG	PROXEN NP 660	Naproxen Sodium	TABLET	ORAL	20231107	N/A	ANDA	ANDA091353	OPMX LLC	NAPROXEN SODIUM	220 mg/1	50 POUCH in 1 CARTON (69729-123-50) / 2 TABLET in 1 POUCH
62207-327-43	62207-327	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20210716	N/A	ANDA	ANDA091353	Granules India Ltd	NAPROXEN SODIUM	220 mg/1	100 TABLET in 1 BOTTLE (62207-327-43)
62207-327-47	62207-327	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20210716	N/A	ANDA	ANDA091353	Granules India Ltd	NAPROXEN SODIUM	220 mg/1	500 TABLET in 1 BOTTLE (62207-327-47)
62207-327-49	62207-327	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20210716	N/A	ANDA	ANDA091353	Granules India Ltd	NAPROXEN SODIUM	220 mg/1	1000 TABLET in 1 BOTTLE (62207-327-49)
62207-328-41	62207-328	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20210716	N/A	ANDA	ANDA091353	Granules India Ltd	NAPROXEN SODIUM	220 mg/1	24 TABLET in 1 BOTTLE (62207-328-41)
62207-328-42	62207-328	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20210716	N/A	ANDA	ANDA091353	Granules India Ltd	NAPROXEN SODIUM	220 mg/1	50 TABLET in 1 BOTTLE (62207-328-42)
62207-328-43	62207-328	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20210716	N/A	ANDA	ANDA091353	Granules India Ltd	NAPROXEN SODIUM	220 mg/1	100 TABLET in 1 BOTTLE (62207-328-43)
62207-328-47	62207-328	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20210716	N/A	ANDA	ANDA091353	Granules India Ltd	NAPROXEN SODIUM	220 mg/1	500 TABLET in 1 BOTTLE (62207-328-47)
62207-328-49	62207-328	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20210716	N/A	ANDA	ANDA091353	Granules India Ltd	NAPROXEN SODIUM	220 mg/1	1000 TABLET in 1 BOTTLE (62207-328-49)
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)