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
71205-469-30	71205-469	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET, DELAYED RELEASE	ORAL	20200814	20250331	ANDA	ANDA075227	Proficient Rx LP	NAPROXEN	375 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-469-30)
71205-469-60	71205-469	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET, DELAYED RELEASE	ORAL	20200814	20250331	ANDA	ANDA075227	Proficient Rx LP	NAPROXEN	375 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-469-60)
71205-469-90	71205-469	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET, DELAYED RELEASE	ORAL	20200814	20250331	ANDA	ANDA075227	Proficient Rx LP	NAPROXEN	375 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-469-90)
0093-1005-01	0093-1005	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET, DELAYED RELEASE	ORAL	19980731	20250331	ANDA	ANDA075227	Teva Pharmaceuticals USA, Inc.	NAPROXEN	375 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (0093-1005-01)
0093-1005-05	0093-1005	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET, DELAYED RELEASE	ORAL	19980731	20250331	ANDA	ANDA075227	Teva Pharmaceuticals USA, Inc.	NAPROXEN	375 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (0093-1005-05)