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
75987-010-03	75987-010	HUMAN PRESCRIPTION DRUG	DUEXIS	Ibuprofen and Famotidine	TABLET, COATED	ORAL	20111205	20250831	NDA	NDA022519	Horizon Therapeutics USA, Inc.	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	90 TABLET, COATED in 1 BOTTLE (75987-010-03)
75987-010-72	75987-010	HUMAN PRESCRIPTION DRUG	DUEXIS	Ibuprofen and Famotidine	TABLET, COATED	ORAL	20111205	20250831	NDA	NDA022519	Horizon Therapeutics USA, Inc.	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	9 BLISTER PACK in 1 CARTON (75987-010-72) / 3 TABLET, COATED in 1 BLISTER PACK
70748-312-09	70748-312	HUMAN PRESCRIPTION DRUG	Ibuprofen and Famotidine	Ibuprofen and Famotidine	TABLET, COATED	ORAL	20210914	N/A	NDA AUTHORIZED GENERIC	NDA022519	Lupin Pharmaceuticals, Inc.	FAMOTIDINE; IBUPROFEN	26.6 mg/1; 800 mg/1	90 TABLET, COATED in 1 BOTTLE (70748-312-09)