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
60760-603-40	60760-603	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191226	N/A	ANDA	ANDA090796	St. Mary's Medical Park Pharmacy	IBUPROFEN	600 mg/1	40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-603-40)
60760-603-60	60760-603	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191021	N/A	ANDA	ANDA090796	St. Mary's Medical Park Pharmacy	IBUPROFEN	600 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-603-60)
60760-603-90	60760-603	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20230206	N/A	ANDA	ANDA090796	St. Mary's Medical Park Pharmacy	IBUPROFEN	600 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-603-90)
68788-7745-8	68788-7745	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200701	N/A	ANDA	ANDA090796	Preferred Pharmaceuticals, Inc.	IBUPROFEN	400 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (68788-7745-8)
68788-7745-9	68788-7745	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200701	N/A	ANDA	ANDA090796	Preferred Pharmaceuticals, Inc.	IBUPROFEN	400 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-7745-9)
68071-4459-6	68071-4459	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20180531	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	600 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (68071-4459-6)
71335-1503-0	71335-1503	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200212	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (71335-1503-0)
71335-1503-1	71335-1503	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200212	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-1503-1)
71335-1503-2	71335-1503	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200212	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-1503-2)
71335-1503-3	71335-1503	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200212	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1503-3)
71335-1503-4	71335-1503	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200212	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (71335-1503-4)
71335-1503-5	71335-1503	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200212	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1503-5)
71335-1503-6	71335-1503	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200212	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1503-6)
71335-1503-7	71335-1503	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200212	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-1503-7)
71335-1503-8	71335-1503	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200212	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (71335-1503-8)
71335-1503-9	71335-1503	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200212	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-1503-9)
51655-275-20	51655-275	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20210709	N/A	ANDA	ANDA090796	Northwind Pharmaceuticals	IBUPROFEN	800 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-20)
51655-275-21	51655-275	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20201029	N/A	ANDA	ANDA090796	Northwind Pharmaceuticals	IBUPROFEN	800 mg/1	21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-21)
51655-275-25	51655-275	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20210217	N/A	ANDA	ANDA090796	Northwind Pharmaceuticals	IBUPROFEN	800 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-25)
51655-275-26	51655-275	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200616	N/A	ANDA	ANDA090796	Northwind Pharmaceuticals	IBUPROFEN	800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-26)