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
36800-368-71	36800-368	HUMAN OTC DRUG	TopCare All Day Pain Relief	Naproxen Sodium	TABLET, FILM COATED	ORAL	19970114	N/A	ANDA	ANDA074661	Topco Associates LLC	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (36800-368-71) / 50 TABLET, FILM COATED in 1 BOTTLE
36800-368-75	36800-368	HUMAN OTC DRUG	TopCare All Day Pain Relief	Naproxen Sodium	TABLET, FILM COATED	ORAL	20220712	N/A	ANDA	ANDA074661	Topco Associates LLC	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (36800-368-75) / 90 TABLET, FILM COATED in 1 BOTTLE
36800-368-76	36800-368	HUMAN OTC DRUG	TopCare All Day Pain Relief	Naproxen Sodium	TABLET, FILM COATED	ORAL	20070629	N/A	ANDA	ANDA074661	Topco Associates LLC	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (36800-368-76) / 120 TABLET, FILM COATED in 1 BOTTLE
36800-368-82	36800-368	HUMAN OTC DRUG	TopCare All Day Pain Relief	Naproxen Sodium	TABLET, FILM COATED	ORAL	20040127	N/A	ANDA	ANDA074661	Topco Associates LLC	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (36800-368-82) / 200 TABLET, FILM COATED in 1 BOTTLE
80267-001-71	80267-001	HUMAN OTC DRUG	betr headache pain relief	naproxen sodium	TABLET, FILM COATED	ORAL	20210209	N/A	ANDA	ANDA074661	Live Betr LLC	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (80267-001-71) / 50 TABLET, FILM COATED in 1 BOTTLE
55910-500-82	55910-500	HUMAN OTC DRUG	dg health naproxen sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20170905	N/A	ANDA	ANDA074661	Dolgencorp Inc	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (55910-500-82) / 200 TABLET, FILM COATED in 1 BOTTLE
41163-511-71	41163-511	HUMAN OTC DRUG	equaline naproxen sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20140924	N/A	ANDA	ANDA074661	United Natural Foods, Inc. dba UNFI	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (41163-511-71) / 50 TABLET, FILM COATED in 1 BOTTLE
41163-511-75	41163-511	HUMAN OTC DRUG	equaline naproxen sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20220921	N/A	ANDA	ANDA074661	United Natural Foods, Inc. dba UNFI	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (41163-511-75) / 90 TABLET, FILM COATED in 1 BOTTLE
41250-477-62	41250-477	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20180706	N/A	ANDA	ANDA074661	Meijer Distribution Inc	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (41250-477-62) / 24 TABLET, FILM COATED in 1 BOTTLE
41250-477-71	41250-477	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20140305	N/A	ANDA	ANDA074661	Meijer Distribution Inc	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (41250-477-71) / 50 TABLET, FILM COATED in 1 BOTTLE
41250-477-75	41250-477	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20220526	N/A	ANDA	ANDA074661	Meijer Distribution Inc	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (41250-477-75) / 90 TABLET, FILM COATED in 1 BOTTLE
41250-477-79	41250-477	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20140305	N/A	ANDA	ANDA074661	Meijer Distribution Inc	NAPROXEN SODIUM	220 mg/1	400 TABLET, FILM COATED in 1 BOTTLE (41250-477-79)
41520-533-71	41520-533	HUMAN OTC DRUG	Care One Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20160708	N/A	ANDA	ANDA074661	American Sales Company	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (41520-533-71) / 50 TABLET, FILM COATED in 1 BOTTLE
50090-0685-1	50090-0685	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20181031	N/A	ANDA	ANDA074661	A-S Medication Solutions	NAPROXEN SODIUM	220 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (50090-0685-1)
0113-4368-75	0113-4368	HUMAN OTC DRUG	Good Sense Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20211208	N/A	ANDA	ANDA074661	L. Perrigo Company	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (0113-4368-75) / 90 TABLET, FILM COATED in 1 BOTTLE
0113-4368-79	0113-4368	HUMAN OTC DRUG	Good Sense Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20180619	N/A	ANDA	ANDA074661	L. Perrigo Company	NAPROXEN SODIUM	220 mg/1	400 TABLET, FILM COATED in 1 BOTTLE (0113-4368-79)
0113-4368-82	0113-4368	HUMAN OTC DRUG	Good Sense Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20260402	N/A	ANDA	ANDA074661	L. Perrigo Company	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (0113-4368-82) / 200 TABLET, FILM COATED in 1 BOTTLE (0113-4368-00)
71335-2584-6	71335-2584	HUMAN OTC DRUG	Good Sense Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20250403	N/A	ANDA	ANDA074661	Bryant Ranch Prepack	NAPROXEN SODIUM	220 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (71335-2584-6)
71335-2584-7	71335-2584	HUMAN OTC DRUG	Good Sense Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20250403	N/A	ANDA	ANDA074661	Bryant Ranch Prepack	NAPROXEN SODIUM	220 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-2584-7)
71335-2584-8	71335-2584	HUMAN OTC DRUG	Good Sense Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20250403	N/A	ANDA	ANDA074661	Bryant Ranch Prepack	NAPROXEN SODIUM	220 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-2584-8)