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
71610-967-60	71610-967	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20251203	N/A	ANDA	ANDA075682	Aphena Pharma Solutions - Tennessee, LLC	IBUPROFEN	800 mg/1	90 TABLET in 1 BOTTLE (71610-967-60)
71610-967-80	71610-967	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20251203	N/A	ANDA	ANDA075682	Aphena Pharma Solutions - Tennessee, LLC	IBUPROFEN	800 mg/1	180 TABLET in 1 BOTTLE (71610-967-80)
71610-967-92	71610-967	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20251203	N/A	ANDA	ANDA075682	Aphena Pharma Solutions - Tennessee, LLC	IBUPROFEN	800 mg/1	270 TABLET in 1 BOTTLE (71610-967-92)
71610-550-80	71610-550	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20210501	N/A	ANDA	ANDA075682	Aphena Pharma Solutions - Tennessee, LLC	IBUPROFEN	800 mg/1	180 TABLET in 1 BOTTLE (71610-550-80)
71610-550-92	71610-550	HUMAN PRESCRIPTION DRUG	IBU	Ibuprofen	TABLET	ORAL	20210501	N/A	ANDA	ANDA075682	Aphena Pharma Solutions - Tennessee, LLC	IBUPROFEN	800 mg/1	270 TABLET in 1 BOTTLE (71610-550-92)