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
55319-717-08	55319-717	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET, FILM COATED	ORAL	20231213	N/A	ANDA	ANDA204872	Family Dollar Services Inc	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (55319-717-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
55319-406-15	55319-406	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET, FILM COATED	ORAL	20231215	N/A	ANDA	ANDA204872	Family Dollar Services Inc	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (55319-406-15) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
57896-954-05	57896-954	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET	ORAL	20190101	N/A	ANDA	ANDA204872	Geri-Care Pharmaceutical Corp	NAPROXEN SODIUM	220 mg/1	50 TABLET in 1 BOTTLE (57896-954-05)
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)
57896-954-01	57896-954	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET	ORAL	20190101	N/A	ANDA	ANDA204872	Geri-Care Pharmaceutical Corp	NAPROXEN SODIUM	220 mg/1	100 TABLET in 1 BOTTLE (57896-954-01)
42961-122-02	42961-122	HUMAN OTC DRUG	First Aid Direct All Day Pain Relief	Naproxen Sodium	TABLET, COATED	ORAL	20230719	N/A	ANDA	ANDA204872	Cintas Corporation	NAPROXEN SODIUM	220 mg/1	25 PACKET in 1 BOX (42961-122-02) / 1 TABLET, COATED in 1 PACKET (42961-122-01)
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
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
79903-005-27	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)
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)
79903-098-06	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
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)
71335-1282-5	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)