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
71335-1925-3	71335-1925	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20210804	N/A	ANDA	ANDA200629	Bryant Ranch Prepack	NAPROXEN SODIUM	275 mg/1	42 TABLET, FILM COATED in 1 BOTTLE (71335-1925-3)
71335-1925-4	71335-1925	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20210804	N/A	ANDA	ANDA200629	Bryant Ranch Prepack	NAPROXEN SODIUM	275 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-1925-4)
71335-1925-5	71335-1925	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20210804	N/A	ANDA	ANDA200629	Bryant Ranch Prepack	NAPROXEN SODIUM	275 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-1925-5)
71335-1925-6	71335-1925	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20210804	N/A	ANDA	ANDA200629	Bryant Ranch Prepack	NAPROXEN SODIUM	275 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1925-6)
50090-3352-3	50090-3352	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20180129	N/A	ANDA	ANDA200629	A-S Medication Solutions	NAPROXEN SODIUM	550 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (50090-3352-3)
50090-3352-5	50090-3352	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20180312	N/A	ANDA	ANDA200629	A-S Medication Solutions	NAPROXEN SODIUM	550 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-3352-5)
50090-3352-6	50090-3352	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20180712	N/A	ANDA	ANDA200629	A-S Medication Solutions	NAPROXEN SODIUM	550 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (50090-3352-6)
53002-5330-1	53002-5330	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20210101	N/A	ANDA	ANDA200629	RPK Pharmaceuticals, Inc.	NAPROXEN SODIUM	550 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (53002-5330-1)
53002-5330-2	53002-5330	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20210101	N/A	ANDA	ANDA200629	RPK Pharmaceuticals, Inc.	NAPROXEN SODIUM	550 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (53002-5330-2)
53002-5330-3	53002-5330	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20210101	N/A	ANDA	ANDA200629	RPK Pharmaceuticals, Inc.	NAPROXEN SODIUM	550 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (53002-5330-3)
65862-515-05	65862-515	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20111031	N/A	ANDA	ANDA200629	Aurobindo Pharma Limited	NAPROXEN SODIUM	275 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-515-05)
65862-515-99	65862-515	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20111031	N/A	ANDA	ANDA200629	Aurobindo Pharma Limited	NAPROXEN SODIUM	275 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-515-99)
65862-516-01	65862-516	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20111031	N/A	ANDA	ANDA200629	Aurobindo Pharma Limited	NAPROXEN SODIUM	550 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-516-01)