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
71335-1282-7	71335-1282	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET	ORAL	20220223	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	20220223	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	20220223	N/A	ANDA	ANDA204872	Bryant Ranch Prepack	NAPROXEN SODIUM	220 mg/1	24 TABLET in 1 BOTTLE (71335-1282-9)
71335-1282-6	71335-1282	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET	ORAL	20220223	N/A	ANDA	ANDA204872	Bryant Ranch Prepack	NAPROXEN SODIUM	220 mg/1	14 TABLET in 1 BOTTLE (71335-1282-6)
71335-1282-5	71335-1282	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET	ORAL	20220223	N/A	ANDA	ANDA204872	Bryant Ranch Prepack	NAPROXEN SODIUM	220 mg/1	60 TABLET in 1 BOTTLE (71335-1282-5)
71335-1282-4	71335-1282	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET	ORAL	20220223	N/A	ANDA	ANDA204872	Bryant Ranch Prepack	NAPROXEN SODIUM	220 mg/1	50 TABLET in 1 BOTTLE (71335-1282-4)
71335-1282-1	71335-1282	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET	ORAL	20220223	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	20220223	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	20220223	N/A	ANDA	ANDA204872	Bryant Ranch Prepack	NAPROXEN SODIUM	220 mg/1	40 TABLET in 1 BOTTLE (71335-1282-3)
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)
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)
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)
50844-471-11	50844-471	HUMAN OTC DRUG	Naproxen Headache Pain	Naproxen Sodium	TABLET, FILM COATED	ORAL	20200916	N/A	ANDA	ANDA204872	L.N.K. International, Inc.	NAPROXEN SODIUM	220 mg/1	60 POUCH in 1 CARTON (50844-471-11) / 1 TABLET, FILM COATED in 1 POUCH (50844-471-43)
50844-471-14	50844-471	HUMAN OTC DRUG	Naproxen Headache Pain	Naproxen Sodium	TABLET, FILM COATED	ORAL	20200916	N/A	ANDA	ANDA204872	L.N.K. International, Inc.	NAPROXEN SODIUM	220 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-471-14)
50844-471-16	50844-471	HUMAN OTC DRUG	Naproxen Headache Pain	Naproxen Sodium	TABLET, FILM COATED	ORAL	20200916	N/A	ANDA	ANDA204872	L.N.K. International, Inc.	NAPROXEN SODIUM	220 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-471-16)
50844-471-19	50844-471	HUMAN OTC DRUG	Naproxen Headache Pain	Naproxen Sodium	TABLET, FILM COATED	ORAL	20200916	N/A	ANDA	ANDA204872	L.N.K. International, Inc.	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (50844-471-19) / 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
50844-471-22	50844-471	HUMAN OTC DRUG	Naproxen Headache Pain	Naproxen Sodium	TABLET, FILM COATED	ORAL	20200916	N/A	ANDA	ANDA204872	L.N.K. International, Inc.	NAPROXEN SODIUM	220 mg/1	48 POUCH in 1 CARTON (50844-471-22) / 1 TABLET, FILM COATED in 1 POUCH (50844-471-43)
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)