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
80425-0532-3	80425-0532	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20250602	N/A	ANDA	ANDA078314	Advanced Rx of Tennessee, LLC	NAPROXEN SODIUM	550 mg/1	90 TABLET in 1 BOTTLE (80425-0532-3)
80425-0532-2	80425-0532	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20250602	N/A	ANDA	ANDA078314	Advanced Rx of Tennessee, LLC	NAPROXEN SODIUM	550 mg/1	60 TABLET in 1 BOTTLE (80425-0532-2)
80425-0532-1	80425-0532	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20250602	N/A	ANDA	ANDA078314	Advanced Rx of Tennessee, LLC	NAPROXEN SODIUM	550 mg/1	30 TABLET in 1 BOTTLE (80425-0532-1)
68462-178-01	68462-178	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20070801	N/A	ANDA	ANDA078314	Glenmark Pharmaceuticals Inc., USA	NAPROXEN SODIUM	275 mg/1	100 TABLET in 1 BOTTLE (68462-178-01)
68462-178-05	68462-178	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20070801	N/A	ANDA	ANDA078314	Glenmark Pharmaceuticals Inc., USA	NAPROXEN SODIUM	275 mg/1	500 TABLET in 1 BOTTLE (68462-178-05)
68462-179-01	68462-179	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20070801	N/A	ANDA	ANDA078314	Glenmark Pharmaceuticals Inc., USA	NAPROXEN SODIUM	550 mg/1	100 TABLET in 1 BOTTLE (68462-179-01)
68462-179-05	68462-179	HUMAN PRESCRIPTION DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20070801	N/A	ANDA	ANDA078314	Glenmark Pharmaceuticals Inc., USA	NAPROXEN SODIUM	550 mg/1	500 TABLET in 1 BOTTLE (68462-179-05)