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
60760-092-14	60760-092	HUMAN PRESCRIPTION DRUG	Oxaprozin	Oxaprozin	TABLET	ORAL	20190821	N/A	ANDA	ANDA208633	St Mary's Medical Park Pharmacy	OXAPROZIN	600 mg/1	14 TABLET in 1 BOTTLE, PLASTIC (60760-092-14)
71335-0617-4	71335-0617	HUMAN PRESCRIPTION DRUG	Oxaprozin	Oxaprozin	TABLET	ORAL	20180214	N/A	ANDA	ANDA208633	Bryant Ranch Prepack	OXAPROZIN	600 mg/1	60 TABLET in 1 BOTTLE (71335-0617-4)
71335-0617-5	71335-0617	HUMAN PRESCRIPTION DRUG	Oxaprozin	Oxaprozin	TABLET	ORAL	20180405	N/A	ANDA	ANDA208633	Bryant Ranch Prepack	OXAPROZIN	600 mg/1	90 TABLET in 1 BOTTLE (71335-0617-5)
71335-0617-6	71335-0617	HUMAN PRESCRIPTION DRUG	Oxaprozin	Oxaprozin	TABLET	ORAL	20211227	N/A	ANDA	ANDA208633	Bryant Ranch Prepack	OXAPROZIN	600 mg/1	6 TABLET in 1 BOTTLE (71335-0617-6)
71335-0617-7	71335-0617	HUMAN PRESCRIPTION DRUG	Oxaprozin	Oxaprozin	TABLET	ORAL	20211227	N/A	ANDA	ANDA208633	Bryant Ranch Prepack	OXAPROZIN	600 mg/1	120 TABLET in 1 BOTTLE (71335-0617-7)
69238-1120-1	69238-1120	HUMAN PRESCRIPTION DRUG	Oxaprozin	Oxaprozin	TABLET	ORAL	20170504	N/A	ANDA	ANDA208633	Amneal Pharmaceuticals NY LLC	OXAPROZIN	600 mg/1	100 TABLET in 1 BOTTLE (69238-1120-1)
69238-1120-5	69238-1120	HUMAN PRESCRIPTION DRUG	Oxaprozin	Oxaprozin	TABLET	ORAL	20170504	N/A	ANDA	ANDA208633	Amneal Pharmaceuticals NY LLC	OXAPROZIN	600 mg/1	500 TABLET in 1 BOTTLE (69238-1120-5)
71335-0617-3	71335-0617	HUMAN PRESCRIPTION DRUG	Oxaprozin	Oxaprozin	TABLET	ORAL	20211227	N/A	ANDA	ANDA208633	Bryant Ranch Prepack	OXAPROZIN	600 mg/1	14 TABLET in 1 BOTTLE (71335-0617-3)
71335-0617-2	71335-0617	HUMAN PRESCRIPTION DRUG	Oxaprozin	Oxaprozin	TABLET	ORAL	20211227	N/A	ANDA	ANDA208633	Bryant Ranch Prepack	OXAPROZIN	600 mg/1	20 TABLET in 1 BOTTLE (71335-0617-2)
71335-0617-1	71335-0617	HUMAN PRESCRIPTION DRUG	Oxaprozin	Oxaprozin	TABLET	ORAL	20211227	N/A	ANDA	ANDA208633	Bryant Ranch Prepack	OXAPROZIN	600 mg/1	30 TABLET in 1 BOTTLE (71335-0617-1)