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
63981-368-79	63981-368	HUMAN OTC DRUG	kirkland signature naproxen sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20070604	N/A	ANDA	ANDA074661	Costco Wholesale Company	NAPROXEN SODIUM	220 mg/1	400 TABLET, FILM COATED in 1 BOTTLE (63981-368-79)
37808-713-79	37808-713	HUMAN OTC DRUG	naproxen sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20171003	N/A	ANDA	ANDA074661	H E B	NAPROXEN SODIUM	220 mg/1	400 TABLET, FILM COATED in 1 BOTTLE (37808-713-79)
11673-909-75	11673-909	HUMAN OTC DRUG	up and up naproxen sodium	naproxen sodium	TABLET, FILM COATED	ORAL	20220210	N/A	ANDA	ANDA074661	Target Corporation	NAPROXEN SODIUM	220 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (11673-909-75)
36800-368-62	36800-368	HUMAN OTC DRUG	TopCare All Day Pain Relief	Naproxen Sodium	TABLET, FILM COATED	ORAL	19970722	N/A	ANDA	ANDA074661	Topco Associates LLC	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (36800-368-62) / 24 TABLET, FILM COATED in 1 BOTTLE
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
63187-596-24	63187-596	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20170901	N/A	ANDA	ANDA074661	Proficient Rx LP	NAPROXEN SODIUM	220 mg/1	24 TABLET, FILM COATED in 1 BOTTLE (63187-596-24)
63187-596-28	63187-596	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20170801	N/A	ANDA	ANDA074661	Proficient Rx LP	NAPROXEN SODIUM	220 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (63187-596-28)
63187-596-30	63187-596	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20150803	N/A	ANDA	ANDA074661	Proficient Rx LP	NAPROXEN SODIUM	220 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-596-30)
63187-596-60	63187-596	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20150803	N/A	ANDA	ANDA074661	Proficient Rx LP	NAPROXEN SODIUM	220 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63187-596-60)
63187-596-90	63187-596	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20150803	N/A	ANDA	ANDA074661	Proficient Rx LP	NAPROXEN SODIUM	220 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63187-596-90)
72789-543-14	72789-543	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20251223	N/A	ANDA	ANDA074661	PD-Rx Pharmaceuticals, Inc.	NAPROXEN SODIUM	220 mg/1	14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-543-14)
72789-543-28	72789-543	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20251223	N/A	ANDA	ANDA074661	PD-Rx Pharmaceuticals, Inc.	NAPROXEN SODIUM	220 mg/1	28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-543-28)
41163-511-62	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 (41163-511-62) / 24 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
50090-3356-0	50090-3356	HUMAN OTC DRUG	rugby all day relief	Naproxen Sodium	TABLET, FILM COATED	ORAL	20180131	N/A	ANDA	ANDA074661	A-S Medication Solutions	NAPROXEN SODIUM	220 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-3356-0)
50090-3356-1	50090-3356	HUMAN OTC DRUG	rugby all day relief	Naproxen Sodium	TABLET, FILM COATED	ORAL	20250313	N/A	ANDA	ANDA074661	A-S Medication Solutions	NAPROXEN SODIUM	220 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (50090-3356-1)
71335-1061-1	71335-1061	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20211228	N/A	ANDA	ANDA074661	Bryant Ranch Prepack	NAPROXEN SODIUM	220 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-1061-1)