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
79903-098-06	79903-098	HUMAN OTC DRUG	All Day Back and Muscle Pain Relief	Naproxen Sodium	TABLET, FILM COATED	ORAL	20220117	20260228	ANDA	ANDA204872	WALMART INC.	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (79903-098-06) / 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
79903-098-52	79903-098	HUMAN OTC DRUG	All Day Back and Muscle Pain Relief	Naproxen Sodium	TABLET, FILM COATED	ORAL	20220117	20260228	ANDA	ANDA204872	WALMART INC.	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (79903-098-52) / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
68071-5039-1	68071-5039	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET	ORAL	20230110	N/A	ANDA	ANDA204872	NuCare Pharmaceuticals,Inc.	NAPROXEN SODIUM	220 mg/1	21 TABLET in 1 BOTTLE (68071-5039-1)
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)
27854-160-01	27854-160	HUMAN OTC DRUG	Flanax	Naproxen Sodium	TABLET, FILM COATED	ORAL	20180115	N/A	ANDA	ANDA204872	Belmora LLC	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (27854-160-01) / 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
27854-160-24	27854-160	HUMAN OTC DRUG	Flanax	Naproxen Sodium	TABLET, FILM COATED	ORAL	20180115	N/A	ANDA	ANDA204872	Belmora LLC	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (27854-160-24) / 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
27854-170-01	27854-170	HUMAN OTC DRUG	AnaDent	Naproxen Sodium	TABLET, FILM COATED	ORAL	20170123	N/A	ANDA	ANDA204872	Belmora LLC	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (27854-170-01) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
46122-562-58	46122-562	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET, FILM COATED	ORAL	20190201	N/A	ANDA	ANDA204872	Amerisource Bergen	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (46122-562-58) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
46122-562-71	46122-562	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET, FILM COATED	ORAL	20190201	N/A	ANDA	ANDA204872	Amerisource Bergen	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (46122-562-71) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
46122-562-78	46122-562	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET, FILM COATED	ORAL	20190201	N/A	ANDA	ANDA204872	Amerisource Bergen	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (46122-562-78) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
46122-564-71	46122-564	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET, FILM COATED	ORAL	20190201	N/A	ANDA	ANDA204872	Amerisource Bergen	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (46122-564-71) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
46122-564-78	46122-564	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET, FILM COATED	ORAL	20190201	N/A	ANDA	ANDA204872	Amerisource Bergen	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (46122-564-78) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
46122-564-81	46122-564	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET, FILM COATED	ORAL	20190201	N/A	ANDA	ANDA204872	Amerisource Bergen	NAPROXEN SODIUM	220 mg/1	200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (46122-564-81)
71141-182-32	71141-182	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20230522	N/A	ANDA	ANDA204872	Lidl US LLC	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (71141-182-32) / 100 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
50844-261-08	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
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)