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
31722-315-90	31722-315	HUMAN PRESCRIPTION DRUG	IBUPROFEN AND FAMOTIDINE	Ibuprofen and famotidine	TABLET	ORAL	20230315	N/A	ANDA	ANDA216814	Camber Pharmaceuticals, Inc.	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	90 TABLET in 1 BOTTLE (31722-315-90)
80425-0384-1	80425-0384	HUMAN PRESCRIPTION DRUG	IBUPROFEN AND FAMOTIDINE	Ibuprofen and famotidine	TABLET	ORAL	20240423	N/A	ANDA	ANDA216814	Advanced Rx Pharmacy of Tennessee, LLC	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	30 TABLET in 1 BOTTLE (80425-0384-1)
80425-0384-2	80425-0384	HUMAN PRESCRIPTION DRUG	IBUPROFEN AND FAMOTIDINE	Ibuprofen and famotidine	TABLET	ORAL	20240423	N/A	ANDA	ANDA216814	Advanced Rx Pharmacy of Tennessee, LLC	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	60 TABLET in 1 BOTTLE (80425-0384-2)
80425-0384-3	80425-0384	HUMAN PRESCRIPTION DRUG	IBUPROFEN AND FAMOTIDINE	Ibuprofen and famotidine	TABLET	ORAL	20240423	N/A	ANDA	ANDA216814	Advanced Rx Pharmacy of Tennessee, LLC	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	90 TABLET in 1 BOTTLE (80425-0384-3)
43602-544-05	43602-544	HUMAN PRESCRIPTION DRUG	IBUPROFEN AND FAMOTIDINE	Ibuprofen and famotidine	TABLET	ORAL	20221006	N/A	ANDA	ANDA216814	Ascent Pharmaceuticals, Inc.	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	500 TABLET in 1 BOTTLE (43602-544-05)
43602-544-30	43602-544	HUMAN PRESCRIPTION DRUG	IBUPROFEN AND FAMOTIDINE	Ibuprofen and famotidine	TABLET	ORAL	20221006	N/A	ANDA	ANDA216814	Ascent Pharmaceuticals, Inc.	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	30 TABLET in 1 BOTTLE (43602-544-30)
43602-544-90	43602-544	HUMAN PRESCRIPTION DRUG	IBUPROFEN AND FAMOTIDINE	Ibuprofen and famotidine	TABLET	ORAL	20221006	N/A	ANDA	ANDA216814	Ascent Pharmaceuticals, Inc.	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	90 TABLET in 1 BOTTLE (43602-544-90)