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
69420-1375-1	69420-1375	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190501	N/A	NDA AUTHORIZED GENERIC	NDA020353	SA3, LLC	NAPROXEN SODIUM	375 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69420-1375-1)
52427-274-30	52427-274	HUMAN PRESCRIPTION DRUG	Naprelan	Naproxen Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20140117	N/A	NDA	NDA020353	ALMATICA PHARMA INC.	NAPROXEN SODIUM	750 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (52427-274-30)
24979-253-68	24979-253	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240425	N/A	NDA AUTHORIZED GENERIC	NDA020353	TWi Pharmaceuticals, Inc.	NAPROXEN SODIUM	500 mg/1	75 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (24979-253-68)
24979-254-06	24979-254	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240425	N/A	NDA AUTHORIZED GENERIC	NDA020353	TWi Pharmaceuticals, Inc.	NAPROXEN SODIUM	750 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (24979-254-06)
52427-273-75	52427-273	HUMAN PRESCRIPTION DRUG	Naprelan	Naproxen Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20140117	N/A	NDA	NDA020353	ALMATICA PHARMA INC.	NAPROXEN SODIUM	500 mg/1	75 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (52427-273-75)
47781-154-75	47781-154	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20150311	N/A	NDA AUTHORIZED GENERIC	NDA020353	Alvogen Inc.	NAPROXEN SODIUM	500 mg/1	75 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47781-154-75)
47781-155-30	47781-155	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20150311	N/A	NDA AUTHORIZED GENERIC	NDA020353	Alvogen Inc.	NAPROXEN SODIUM	750 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47781-155-30)
52427-272-01	52427-272	HUMAN PRESCRIPTION DRUG	Naprelan	Naproxen Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20140117	N/A	NDA	NDA020353	ALMATICA PHARMA INC.	NAPROXEN SODIUM	375 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (52427-272-01)
47781-153-01	47781-153	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20150311	N/A	NDA AUTHORIZED GENERIC	NDA020353	Alvogen Inc.	NAPROXEN SODIUM	375 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47781-153-01)
24979-252-01	24979-252	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240425	N/A	NDA AUTHORIZED GENERIC	NDA020353	TWi Pharmaceuticals, Inc.	NAPROXEN SODIUM	375 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (24979-252-01)