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
49884-366-09	49884-366	HUMAN PRESCRIPTION DRUG	Ibuprofen and famotidine	Ibuprofen and famotidine	TABLET	ORAL	20240322	N/A	ANDA	ANDA203658	ENDO USA, Inc.	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	90 TABLET in 1 BOTTLE (49884-366-09)
80425-0483-1	80425-0483	HUMAN PRESCRIPTION DRUG	Ibuprofen and famotidine	Ibuprofen and famotidine	TABLET	ORAL	20240322	N/A	ANDA	ANDA203658	Advanced Rx of Tennessee, LLC	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	30 TABLET in 1 BOTTLE (80425-0483-1)
80425-0483-2	80425-0483	HUMAN PRESCRIPTION DRUG	Ibuprofen and famotidine	Ibuprofen and famotidine	TABLET	ORAL	20240322	N/A	ANDA	ANDA203658	Advanced Rx of Tennessee, LLC	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	60 TABLET in 1 BOTTLE (80425-0483-2)
80425-0483-3	80425-0483	HUMAN PRESCRIPTION DRUG	Ibuprofen and famotidine	Ibuprofen and famotidine	TABLET	ORAL	20240322	N/A	ANDA	ANDA203658	Advanced Rx of Tennessee, LLC	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	90 TABLET in 1 BOTTLE (80425-0483-3)