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
72189-641-90	72189-641	HUMAN PRESCRIPTION DRUG	Ibuprofen Famotidine	Ibuprofen Famotidine	TABLET, FILM COATED	ORAL	20250918	N/A	ANDA	ANDA211890	Direct_Rx	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72189-641-90)
80425-0422-1	80425-0422	HUMAN PRESCRIPTION DRUG	Ibuprofen and famotidine	Ibuprofen and famotidine	TABLET, FILM COATED	ORAL	20240716	N/A	ANDA	ANDA211890	Advanced Rx of Tennessee, LLC	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0422-1)
80425-0422-2	80425-0422	HUMAN PRESCRIPTION DRUG	Ibuprofen and famotidine	Ibuprofen and famotidine	TABLET, FILM COATED	ORAL	20240716	N/A	ANDA	ANDA211890	Advanced Rx of Tennessee, LLC	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0422-2)
80425-0422-3	80425-0422	HUMAN PRESCRIPTION DRUG	Ibuprofen and famotidine	Ibuprofen and famotidine	TABLET, FILM COATED	ORAL	20240716	N/A	ANDA	ANDA211890	Advanced Rx of Tennessee, LLC	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (80425-0422-3)
85509-1010-3	85509-1010	HUMAN PRESCRIPTION DRUG	Ibuprofen and famotidine	Ibuprofen and famotidine	TABLET, FILM COATED	ORAL	20250721	N/A	ANDA	ANDA211890	PHOENIX RX LLC	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (85509-1010-3)
85509-1010-6	85509-1010	HUMAN PRESCRIPTION DRUG	Ibuprofen and famotidine	Ibuprofen and famotidine	TABLET, FILM COATED	ORAL	20250721	N/A	ANDA	ANDA211890	PHOENIX RX LLC	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (85509-1010-6)
85509-1010-9	85509-1010	HUMAN PRESCRIPTION DRUG	Ibuprofen and famotidine	Ibuprofen and famotidine	TABLET, FILM COATED	ORAL	20250721	N/A	ANDA	ANDA211890	PHOENIX RX LLC	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (85509-1010-9)
67877-626-01	67877-626	HUMAN PRESCRIPTION DRUG	Ibuprofen and famotidine	Ibuprofen and famotidine	TABLET, FILM COATED	ORAL	20210804	N/A	ANDA	ANDA211890	Ascend Laboratories, LLC	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (67877-626-01)
67877-626-05	67877-626	HUMAN PRESCRIPTION DRUG	Ibuprofen and famotidine	Ibuprofen and famotidine	TABLET, FILM COATED	ORAL	20210804	N/A	ANDA	ANDA211890	Ascend Laboratories, LLC	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (67877-626-05)
67877-626-06	67877-626	HUMAN PRESCRIPTION DRUG	Ibuprofen and famotidine	Ibuprofen and famotidine	TABLET, FILM COATED	ORAL	20210804	N/A	ANDA	ANDA211890	Ascend Laboratories, LLC	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	6 BLISTER PACK in 1 CARTON (67877-626-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK
67877-626-90	67877-626	HUMAN PRESCRIPTION DRUG	Ibuprofen and famotidine	Ibuprofen and famotidine	TABLET, FILM COATED	ORAL	20210804	N/A	ANDA	ANDA211890	Ascend Laboratories, LLC	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (67877-626-90)
63629-8891-1	63629-8891	HUMAN PRESCRIPTION DRUG	Ibuprofen and famotidine	Ibuprofen and famotidine	TABLET, FILM COATED	ORAL	20211026	N/A	ANDA	ANDA211890	Bryant Ranch Prepack	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63629-8891-1)
63629-8891-2	63629-8891	HUMAN PRESCRIPTION DRUG	Ibuprofen and famotidine	Ibuprofen and famotidine	TABLET, FILM COATED	ORAL	20220408	N/A	ANDA	ANDA211890	Bryant Ranch Prepack	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63629-8891-2)
63629-8891-3	63629-8891	HUMAN PRESCRIPTION DRUG	Ibuprofen and famotidine	Ibuprofen and famotidine	TABLET, FILM COATED	ORAL	20230915	N/A	ANDA	ANDA211890	Bryant Ranch Prepack	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63629-8891-3)
69306-266-30	69306-266	HUMAN PRESCRIPTION DRUG	Ibuprofen and famotidine	Ibuprofen and famotidine	TABLET, FILM COATED	ORAL	20220830	N/A	ANDA	ANDA211890	Doc Rx	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (69306-266-30)
68788-8897-9	68788-8897	HUMAN PRESCRIPTION DRUG	Ibuprofen and famotidine	Ibuprofen and famotidine	TABLET, FILM COATED	ORAL	20250801	N/A	ANDA	ANDA211890	Preferred Pharmaceuticals Inc.	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-8897-9)
76420-891-01	76420-891	HUMAN PRESCRIPTION DRUG	Ibuprofen and famotidine	Ibuprofen and famotidine	TABLET, FILM COATED	ORAL	20250102	N/A	ANDA	ANDA211890	Asclemed USA, Inc.	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (76420-891-01)
76420-891-05	76420-891	HUMAN PRESCRIPTION DRUG	Ibuprofen and famotidine	Ibuprofen and famotidine	TABLET, FILM COATED	ORAL	20250102	N/A	ANDA	ANDA211890	Asclemed USA, Inc.	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (76420-891-05)
76420-891-06	76420-891	HUMAN PRESCRIPTION DRUG	Ibuprofen and famotidine	Ibuprofen and famotidine	TABLET, FILM COATED	ORAL	20250102	N/A	ANDA	ANDA211890	Asclemed USA, Inc.	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	6 BLISTER PACK in 1 CARTON (76420-891-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK
76420-891-30	76420-891	HUMAN PRESCRIPTION DRUG	Ibuprofen and famotidine	Ibuprofen and famotidine	TABLET, FILM COATED	ORAL	20250102	N/A	ANDA	ANDA211890	Asclemed USA, Inc.	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-891-30)