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
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)
76420-891-60	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	60 TABLET, FILM COATED in 1 BOTTLE (76420-891-60)
76420-891-90	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	90 TABLET, FILM COATED in 1 BOTTLE (76420-891-90)
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)
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)