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
60760-382-14	60760-382	HUMAN PRESCRIPTION DRUG	Oxaprozin	Oxaprozin	TABLET, FILM COATED	ORAL	20220815	N/A	ANDA	ANDA075855	ST MARY'S MEDICAL PARK PHARMACY	OXAPROZIN	600 mg/1	14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-382-14)
72189-595-60	72189-595	HUMAN PRESCRIPTION DRUG	Oxaprozin	Oxaprozin	TABLET, FILM COATED	ORAL	20241202	N/A	ANDA	ANDA075855	Direct_Rx	OXAPROZIN	600 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72189-595-60)
55111-170-01	55111-170	HUMAN PRESCRIPTION DRUG	Oxaprozin	Oxaprozin	TABLET, FILM COATED	ORAL	20010131	N/A	ANDA	ANDA075855	Dr. Reddy's Laboratories Limited	OXAPROZIN	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (55111-170-01)
55111-170-05	55111-170	HUMAN PRESCRIPTION DRUG	Oxaprozin	Oxaprozin	TABLET, FILM COATED	ORAL	20010131	N/A	ANDA	ANDA075855	Dr. Reddy's Laboratories Limited	OXAPROZIN	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (55111-170-05)
71335-0393-1	71335-0393	HUMAN PRESCRIPTION DRUG	Oxaprozin	Oxaprozin	TABLET, FILM COATED	ORAL	20070912	N/A	ANDA	ANDA075855	Bryant Ranch Prepack	OXAPROZIN	600 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0393-1)
71335-0393-2	71335-0393	HUMAN PRESCRIPTION DRUG	Oxaprozin	Oxaprozin	TABLET, FILM COATED	ORAL	20070912	N/A	ANDA	ANDA075855	Bryant Ranch Prepack	OXAPROZIN	600 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-0393-2)
71335-0393-3	71335-0393	HUMAN PRESCRIPTION DRUG	Oxaprozin	Oxaprozin	TABLET, FILM COATED	ORAL	20070912	N/A	ANDA	ANDA075855	Bryant Ranch Prepack	OXAPROZIN	600 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (71335-0393-3)
71335-0393-4	71335-0393	HUMAN PRESCRIPTION DRUG	Oxaprozin	Oxaprozin	TABLET, FILM COATED	ORAL	20070912	N/A	ANDA	ANDA075855	Bryant Ranch Prepack	OXAPROZIN	600 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0393-4)
71335-0393-5	71335-0393	HUMAN PRESCRIPTION DRUG	Oxaprozin	Oxaprozin	TABLET, FILM COATED	ORAL	20070912	N/A	ANDA	ANDA075855	Bryant Ranch Prepack	OXAPROZIN	600 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0393-5)
71335-0393-6	71335-0393	HUMAN PRESCRIPTION DRUG	Oxaprozin	Oxaprozin	TABLET, FILM COATED	ORAL	20070912	N/A	ANDA	ANDA075855	Bryant Ranch Prepack	OXAPROZIN	600 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (71335-0393-6)
71335-0393-7	71335-0393	HUMAN PRESCRIPTION DRUG	Oxaprozin	Oxaprozin	TABLET, FILM COATED	ORAL	20070912	N/A	ANDA	ANDA075855	Bryant Ranch Prepack	OXAPROZIN	600 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-0393-7)