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
71335-0822-3	71335-0822	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20180823	N/A	ANDA	ANDA200629	Bryant Ranch Prepack	NAPROXEN SODIUM	550 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0822-3)
71335-0822-4	71335-0822	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20180529	N/A	ANDA	ANDA200629	Bryant Ranch Prepack	NAPROXEN SODIUM	550 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-0822-4)
71335-0822-5	71335-0822	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20180426	N/A	ANDA	ANDA200629	Bryant Ranch Prepack	NAPROXEN SODIUM	550 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0822-5)
71335-0822-6	71335-0822	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20250129	N/A	ANDA	ANDA200629	Bryant Ranch Prepack	NAPROXEN SODIUM	550 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0822-6)
71335-0822-7	71335-0822	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20250129	N/A	ANDA	ANDA200629	Bryant Ranch Prepack	NAPROXEN SODIUM	550 mg/1	42 TABLET, FILM COATED in 1 BOTTLE (71335-0822-7)
71335-0822-8	71335-0822	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20250129	N/A	ANDA	ANDA200629	Bryant Ranch Prepack	NAPROXEN SODIUM	550 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (71335-0822-8)
71335-0822-9	71335-0822	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20250129	N/A	ANDA	ANDA200629	Bryant Ranch Prepack	NAPROXEN SODIUM	550 mg/1	56 TABLET, FILM COATED in 1 BOTTLE (71335-0822-9)