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
50844-604-99	50844-604	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20170201	N/A	ANDA	ANDA204872	L.N.K. International, Inc.	NAPROXEN SODIUM	220 mg/1	8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-99)
71205-595-24	71205-595	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET	ORAL	20230728	N/A	ANDA	ANDA204872	Proficient Rx LP	NAPROXEN SODIUM	220 mg/1	24 TABLET in 1 BOTTLE (71205-595-24)
71205-595-30	71205-595	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET	ORAL	20210727	N/A	ANDA	ANDA204872	Proficient Rx LP	NAPROXEN SODIUM	220 mg/1	30 TABLET in 1 BOTTLE (71205-595-30)
21130-674-52	21130-674	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET, FILM COATED	ORAL	20231004	N/A	ANDA	ANDA204872	Better Living Brands, LLC	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (21130-674-52) / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
21130-856-52	21130-856	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20231011	N/A	ANDA	ANDA204872	Better Living Brands, LLC	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (21130-856-52) / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
66715-5428-4	66715-5428	HUMAN OTC DRUG	24/7 Life by 7-Eleven Naproxen Sodium	naproxen sodium tablet, film coated	TABLET, FILM COATED	ORAL	20220419	N/A	ANDA	ANDA204872	Lil' Drug Store Products, Inc.	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (66715-5428-4) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
27854-165-10	27854-165	HUMAN OTC DRUG	Flanax Menstrual Pain Reliever	Naproxen Sodium	TABLET, FILM COATED	ORAL	20170123	N/A	ANDA	ANDA204872	Belmora LLC	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (27854-165-10) / 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
59428-604-08	59428-604	HUMAN OTC DRUG	All Day Pain Relief	Naproxen Sodium	TABLET, FILM COATED	ORAL	20201022	N/A	ANDA	ANDA204872	Zapotol Products Corp	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (59428-604-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
50844-417-56	50844-417	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20170201	N/A	ANDA	ANDA204872	L.N.K. International, Inc.	NAPROXEN SODIUM	220 mg/1	25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-56)
50844-417-98	50844-417	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20170201	N/A	ANDA	ANDA204872	L.N.K. International, Inc.	NAPROXEN SODIUM	220 mg/1	8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-98)
50844-417-99	50844-417	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20170201	N/A	ANDA	ANDA204872	L.N.K. International, Inc.	NAPROXEN SODIUM	220 mg/1	8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-99)
53185-604-12	53185-604	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20220311	N/A	ANDA	ANDA204872	Athlete's Needs Inc	NAPROXEN SODIUM	220 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53185-604-12)
53185-604-15	53185-604	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20220311	N/A	ANDA	ANDA204872	Athlete's Needs Inc	NAPROXEN SODIUM	220 mg/1	50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53185-604-15)
79903-005-20	79903-005	HUMAN OTC DRUG	All Day Pain Relief	Naproxen Sodium	TABLET, FILM COATED	ORAL	20201022	N/A	ANDA	ANDA204872	WALMART INC.	NAPROXEN SODIUM	220 mg/1	200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-20)
79903-005-25	79903-005	HUMAN OTC DRUG	All Day Pain Relief	Naproxen Sodium	TABLET, FILM COATED	ORAL	20201022	N/A	ANDA	ANDA204872	WALMART INC.	NAPROXEN SODIUM	220 mg/1	225 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-25)
79903-005-27	79903-005	HUMAN OTC DRUG	All Day Pain Relief	Naproxen Sodium	TABLET, FILM COATED	ORAL	20201022	N/A	ANDA	ANDA204872	WALMART INC.	NAPROXEN SODIUM	220 mg/1	270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-27)
79903-005-90	79903-005	HUMAN OTC DRUG	All Day Pain Relief	Naproxen Sodium	TABLET, FILM COATED	ORAL	20201022	N/A	ANDA	ANDA204872	WALMART INC.	NAPROXEN SODIUM	220 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-90)
71205-595-60	71205-595	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET	ORAL	20210727	N/A	ANDA	ANDA204872	Proficient Rx LP	NAPROXEN SODIUM	220 mg/1	60 TABLET in 1 BOTTLE (71205-595-60)
71205-595-90	71205-595	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET	ORAL	20210727	N/A	ANDA	ANDA204872	Proficient Rx LP	NAPROXEN SODIUM	220 mg/1	90 TABLET in 1 BOTTLE (71205-595-90)
71335-1282-1	71335-1282	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET	ORAL	20211118	N/A	ANDA	ANDA204872	Bryant Ranch Prepack	NAPROXEN SODIUM	220 mg/1	20 TABLET in 1 BOTTLE (71335-1282-1)