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
71335-1650-8	71335-1650	HUMAN PRESCRIPTION DRUG	Naproxen sodium	Naproxen sodium	TABLET, FILM COATED	ORAL	20240812	N/A	ANDA	ANDA078486	Bryant Ranch Prepack	NAPROXEN SODIUM	550 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (71335-1650-8)
71335-1650-9	71335-1650	HUMAN PRESCRIPTION DRUG	Naproxen sodium	Naproxen sodium	TABLET, FILM COATED	ORAL	20240812	N/A	ANDA	ANDA078486	Bryant Ranch Prepack	NAPROXEN SODIUM	550 mg/1	56 TABLET, FILM COATED in 1 BOTTLE (71335-1650-9)
85509-1495-3	85509-1495	HUMAN PRESCRIPTION DRUG	Naproxen sodium	Naproxen sodium	TABLET, FILM COATED	ORAL	20260107	N/A	ANDA	ANDA078486	PHOENIX RX LLC	NAPROXEN SODIUM	550 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (85509-1495-3)
71335-1650-1	71335-1650	HUMAN PRESCRIPTION DRUG	Naproxen sodium	Naproxen sodium	TABLET, FILM COATED	ORAL	20240812	N/A	ANDA	ANDA078486	Bryant Ranch Prepack	NAPROXEN SODIUM	550 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-1650-1)
71335-1650-0	71335-1650	HUMAN PRESCRIPTION DRUG	Naproxen sodium	Naproxen sodium	TABLET, FILM COATED	ORAL	20240812	N/A	ANDA	ANDA078486	Bryant Ranch Prepack	NAPROXEN SODIUM	550 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (71335-1650-0)