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
80425-0089-1	80425-0089	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	Advanced Rx of Tennessee, LLC	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0089-1)
80425-0089-2	80425-0089	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	Advanced Rx of Tennessee, LLC	IBUPROFEN	800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (80425-0089-2)
80425-0089-3	80425-0089	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	Advanced Rx of Tennessee, LLC	IBUPROFEN	800 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (80425-0089-3)
80425-0089-4	80425-0089	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	Advanced Rx of Tennessee, LLC	IBUPROFEN	800 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0089-4)
51655-275-20	51655-275	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20210709	N/A	ANDA	ANDA090796	Northwind Health Company, LLC	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 Health Company, LLC	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 Health Company, LLC	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 Health Company, LLC	IBUPROFEN	800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-26)
51655-275-54	51655-275	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20200921	N/A	ANDA	ANDA090796	Northwind Health Company, LLC	IBUPROFEN	800 mg/1	15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-54)
71335-1396-0	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	84 TABLET, FILM COATED in 1 BOTTLE (71335-1396-0)
71335-1396-1	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-1396-1)
71335-1396-2	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-1396-2)
71335-1396-3	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (71335-1396-3)
71335-1396-4	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (71335-1396-4)
71335-1396-5	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1396-5)
71335-1396-6	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1396-6)
71335-1396-7	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-1396-7)
71335-1396-8	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-1396-8)
70518-2432-1	70518-2432	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20210526	N/A	ANDA	ANDA090796	REMEDYREPACK INC.	IBUPROFEN	400 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2432-1)
60760-603-20	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	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-603-20)