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
69367-401-10	69367-401	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, COATED	ORAL	20240909	N/A	ANDA	ANDA217669	Westminster Pharmaceuticals, LLC	FAMOTIDINE	40 mg/1	1000 TABLET, COATED in 1 BOTTLE, PLASTIC (69367-401-10)
10267-5689-5	10267-5689	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, COATED	ORAL	20240831	N/A	ANDA	ANDA217669	Contract Pharmacal Corp.	FAMOTIDINE	20 mg/1	500 TABLET, COATED in 1 BOTTLE (10267-5689-5)
10267-5690-4	10267-5690	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, COATED	ORAL	20240831	N/A	ANDA	ANDA217669	Contract Pharmacal Corp.	FAMOTIDINE	40 mg/1	1000 TABLET, COATED in 1 BOTTLE (10267-5690-4)
10267-5690-5	10267-5690	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, COATED	ORAL	20240831	N/A	ANDA	ANDA217669	Contract Pharmacal Corp.	FAMOTIDINE	40 mg/1	500 TABLET, COATED in 1 BOTTLE (10267-5690-5)
10267-5690-1	10267-5690	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, COATED	ORAL	20240831	N/A	ANDA	ANDA217669	Contract Pharmacal Corp.	FAMOTIDINE	40 mg/1	100 TABLET, COATED in 1 BOTTLE (10267-5690-1)
10267-5689-1	10267-5689	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, COATED	ORAL	20240831	N/A	ANDA	ANDA217669	Contract Pharmacal Corp.	FAMOTIDINE	20 mg/1	100 TABLET, COATED in 1 BOTTLE (10267-5689-1)
10267-5689-4	10267-5689	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, COATED	ORAL	20240831	N/A	ANDA	ANDA217669	Contract Pharmacal Corp.	FAMOTIDINE	20 mg/1	1000 TABLET, COATED in 1 BOTTLE (10267-5689-4)