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
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
50844-604-06	50844-604	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20260219	N/A	ANDA	ANDA204872	L.N.K. International, Inc.	NAPROXEN SODIUM	220 mg/1	200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-06)
50844-604-09	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	4 BLISTER PACK in 1 CARTON (50844-604-09) / 5 TABLET, FILM COATED in 1 BLISTER PACK
50844-604-14	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	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-14)
50844-604-15	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	1 BOTTLE, PLASTIC in 1 CARTON (50844-604-15) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
50844-604-16	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	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-16)
50844-604-19	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	1 BOTTLE, PLASTIC in 1 CARTON (50844-604-19) / 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
50844-604-56	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	25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-56)
51316-817-08	51316-817	HUMAN OTC DRUG	Back and Muscle Pain	Naproxen Sodium	TABLET, FILM COATED	ORAL	20220418	N/A	ANDA	ANDA204872	CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (51316-817-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
51316-817-52	51316-817	HUMAN OTC DRUG	Back and Muscle Pain	Naproxen Sodium	TABLET, FILM COATED	ORAL	20220418	N/A	ANDA	ANDA204872	CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (51316-817-52) / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
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)
50844-471-56	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	25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-471-56)
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)