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
71335-1925-4	71335-1925	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20250130	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	20250130	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	20210729	N/A	ANDA	ANDA200629	Bryant Ranch Prepack	NAPROXEN SODIUM	275 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1925-6)
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)
65862-516-05	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	500 TABLET, FILM COATED in 1 BOTTLE (65862-516-05)
65862-516-26	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	2500 TABLET, FILM COATED in 1 BOTTLE (65862-516-26)
65862-516-30	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	30 TABLET, FILM COATED in 1 BOTTLE (65862-516-30)