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
69230-329-01	69230-329	HUMAN OTC DRUG	Naproxen sodium	Naproxen sodium	TABLET, FILM COATED	ORAL	20221028	N/A	ANDA	ANDA211065	Camber Consumer Care Inc	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (69230-329-01) / 100 TABLET, FILM COATED in 1 BOTTLE
69230-329-02	69230-329	HUMAN OTC DRUG	Naproxen sodium	Naproxen sodium	TABLET, FILM COATED	ORAL	20221028	N/A	ANDA	ANDA211065	Camber Consumer Care Inc	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (69230-329-02) / 200 TABLET, FILM COATED in 1 BOTTLE
69230-329-05	69230-329	HUMAN OTC DRUG	Naproxen sodium	Naproxen sodium	TABLET, FILM COATED	ORAL	20221028	N/A	ANDA	ANDA211065	Camber Consumer Care Inc	NAPROXEN SODIUM	220 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (69230-329-05)
69230-329-10	69230-329	HUMAN OTC DRUG	Naproxen sodium	Naproxen sodium	TABLET, FILM COATED	ORAL	20221028	N/A	ANDA	ANDA211065	Camber Consumer Care Inc	NAPROXEN SODIUM	220 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (69230-329-10)
69230-329-24	69230-329	HUMAN OTC DRUG	Naproxen sodium	Naproxen sodium	TABLET, FILM COATED	ORAL	20221028	N/A	ANDA	ANDA211065	Camber Consumer Care Inc	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (69230-329-24) / 24 TABLET, FILM COATED in 1 BOTTLE
69230-329-50	69230-329	HUMAN OTC DRUG	Naproxen sodium	Naproxen sodium	TABLET, FILM COATED	ORAL	20221028	N/A	ANDA	ANDA211065	Camber Consumer Care Inc	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (69230-329-50) / 50 TABLET, FILM COATED in 1 BOTTLE