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
67296-0877-1	67296-0877	HUMAN PRESCRIPTION DRUG	IBU	IBU	TABLET	ORAL	20081120	N/A	ANDA	ANDA075682	RedPharm Drug, Inc.	IBUPROFEN	800 mg/1	10 TABLET in 1 BOTTLE (67296-0877-1)
67296-0877-2	67296-0877	HUMAN PRESCRIPTION DRUG	IBU	IBU	TABLET	ORAL	20081120	N/A	ANDA	ANDA075682	RedPharm Drug, Inc.	IBUPROFEN	800 mg/1	20 TABLET in 1 BOTTLE (67296-0877-2)
67296-0877-3	67296-0877	HUMAN PRESCRIPTION DRUG	IBU	IBU	TABLET	ORAL	20081120	N/A	ANDA	ANDA075682	RedPharm Drug, Inc.	IBUPROFEN	800 mg/1	30 TABLET in 1 BOTTLE (67296-0877-3)
67296-0877-6	67296-0877	HUMAN PRESCRIPTION DRUG	IBU	IBU	TABLET	ORAL	20081120	N/A	ANDA	ANDA075682	RedPharm Drug, Inc.	IBUPROFEN	800 mg/1	60 TABLET in 1 BOTTLE (67296-0877-6)
67296-0913-1	67296-0913	HUMAN PRESCRIPTION DRUG	IBU	IBU	TABLET	ORAL	20081120	N/A	ANDA	ANDA075682	RedPharm Drug, Inc.	IBUPROFEN	600 mg/1	30 TABLET in 1 BOTTLE (67296-0913-1)
67296-0913-3	67296-0913	HUMAN PRESCRIPTION DRUG	IBU	IBU	TABLET	ORAL	20081120	N/A	ANDA	ANDA075682	RedPharm Drug, Inc.	IBUPROFEN	600 mg/1	10 TABLET in 1 BOTTLE (67296-0913-3)
67296-0913-9	67296-0913	HUMAN PRESCRIPTION DRUG	IBU	IBU	TABLET	ORAL	20081120	N/A	ANDA	ANDA075682	RedPharm Drug, Inc.	IBUPROFEN	600 mg/1	90 TABLET in 1 BOTTLE (67296-0913-9)
67296-1217-2	67296-1217	HUMAN PRESCRIPTION DRUG	IBU	IBU	TABLET	ORAL	20081120	N/A	ANDA	ANDA075682	RedPharm Drug, Inc.	IBUPROFEN	400 mg/1	20 TABLET in 1 BOTTLE (67296-1217-2)
67296-1217-3	67296-1217	HUMAN PRESCRIPTION DRUG	IBU	IBU	TABLET	ORAL	20081120	N/A	ANDA	ANDA075682	RedPharm Drug, Inc.	IBUPROFEN	400 mg/1	30 TABLET in 1 BOTTLE (67296-1217-3)
68071-3053-0	68071-3053	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20180316	N/A	ANDA	ANDA075682	NuCare Pharmaceuticals,Inc.	IBUPROFEN	800 mg/1	12 TABLET in 1 BOTTLE (68071-3053-0)
68071-3053-1	68071-3053	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20180316	N/A	ANDA	ANDA075682	NuCare Pharmaceuticals,Inc.	IBUPROFEN	800 mg/1	120 TABLET in 1 BOTTLE (68071-3053-1)
68071-3053-2	68071-3053	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20180316	N/A	ANDA	ANDA075682	NuCare Pharmaceuticals,Inc.	IBUPROFEN	800 mg/1	20 TABLET in 1 BOTTLE (68071-3053-2)
68071-3053-4	68071-3053	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20180316	N/A	ANDA	ANDA075682	NuCare Pharmaceuticals,Inc.	IBUPROFEN	800 mg/1	40 TABLET in 1 BOTTLE (68071-3053-4)
68071-3053-6	68071-3053	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20180316	N/A	ANDA	ANDA075682	NuCare Pharmaceuticals,Inc.	IBUPROFEN	800 mg/1	60 TABLET in 1 BOTTLE (68071-3053-6)
71610-275-60	71610-275	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20190508	N/A	ANDA	ANDA075682	Aphena Pharma Solutions - Tennessee, LLC	IBUPROFEN	800 mg/1	90 TABLET in 1 BOTTLE (71610-275-60)
71610-275-80	71610-275	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20190508	N/A	ANDA	ANDA075682	Aphena Pharma Solutions - Tennessee, LLC	IBUPROFEN	800 mg/1	180 TABLET in 1 BOTTLE (71610-275-80)
71610-275-92	71610-275	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20190508	N/A	ANDA	ANDA075682	Aphena Pharma Solutions - Tennessee, LLC	IBUPROFEN	800 mg/1	270 TABLET in 1 BOTTLE (71610-275-92)
71205-604-15	71205-604	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20210927	N/A	ANDA	ANDA075682	Proficient Rx LP	IBUPROFEN	400 mg/1	15 TABLET in 1 BOTTLE (71205-604-15)
71205-604-20	71205-604	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20210927	N/A	ANDA	ANDA075682	Proficient Rx LP	IBUPROFEN	400 mg/1	20 TABLET in 1 BOTTLE (71205-604-20)
71205-604-21	71205-604	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20210927	N/A	ANDA	ANDA075682	Proficient Rx LP	IBUPROFEN	400 mg/1	21 TABLET in 1 BOTTLE (71205-604-21)