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
71335-1282-1	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)
71335-1282-2	71335-1282	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET	ORAL	20190827	N/A	ANDA	ANDA204872	Bryant Ranch Prepack	NAPROXEN SODIUM	220 mg/1	30 TABLET in 1 BOTTLE (71335-1282-2)
71335-1282-3	71335-1282	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET	ORAL	20191022	N/A	ANDA	ANDA204872	Bryant Ranch Prepack	NAPROXEN SODIUM	220 mg/1	40 TABLET in 1 BOTTLE (71335-1282-3)
71335-1282-4	71335-1282	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET	ORAL	20250110	N/A	ANDA	ANDA204872	Bryant Ranch Prepack	NAPROXEN SODIUM	220 mg/1	50 TABLET in 1 BOTTLE (71335-1282-4)
71335-1282-5	71335-1282	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET	ORAL	20250130	N/A	ANDA	ANDA204872	Bryant Ranch Prepack	NAPROXEN SODIUM	220 mg/1	60 TABLET in 1 BOTTLE (71335-1282-5)
71335-1282-6	71335-1282	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET	ORAL	20191126	N/A	ANDA	ANDA204872	Bryant Ranch Prepack	NAPROXEN SODIUM	220 mg/1	14 TABLET in 1 BOTTLE (71335-1282-6)
71335-1282-7	71335-1282	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET	ORAL	20191025	N/A	ANDA	ANDA204872	Bryant Ranch Prepack	NAPROXEN SODIUM	220 mg/1	100 TABLET in 1 BOTTLE (71335-1282-7)
71335-1282-8	71335-1282	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET	ORAL	20250130	N/A	ANDA	ANDA204872	Bryant Ranch Prepack	NAPROXEN SODIUM	220 mg/1	90 TABLET in 1 BOTTLE (71335-1282-8)
71335-1282-9	71335-1282	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET	ORAL	20250130	N/A	ANDA	ANDA204872	Bryant Ranch Prepack	NAPROXEN SODIUM	220 mg/1	24 TABLET in 1 BOTTLE (71335-1282-9)
50844-261-08	50844-261	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET, FILM COATED	ORAL	20190806	N/A	ANDA	ANDA204872	L.N.K. International, Inc.	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (50844-261-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
79903-005-10	79903-005	HUMAN OTC DRUG	All Day Pain Relief	Naproxen Sodium	TABLET, FILM COATED	ORAL	20201022	20260228	ANDA	ANDA204872	WALMART INC.	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (79903-005-10) / 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
79903-005-12	79903-005	HUMAN OTC DRUG	All Day Pain Relief	Naproxen Sodium	TABLET, FILM COATED	ORAL	20201022	20260228	ANDA	ANDA204872	WALMART INC.	NAPROXEN SODIUM	220 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-12)
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)
79903-005-99	79903-005	HUMAN OTC DRUG	All Day Pain Relief	Naproxen Sodium	TABLET, FILM COATED	ORAL	20201022	20260228	ANDA	ANDA204872	WALMART INC.	NAPROXEN SODIUM	220 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-99)
50844-417-11	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	60 POUCH in 1 CARTON (50844-417-11) / 1 TABLET, FILM COATED in 1 POUCH (50844-417-43)
50844-417-14	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	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-14)
50844-417-16	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	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-16)