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
59651-823-01	59651-823	HUMAN PRESCRIPTION DRUG	CIMETIDINE	CIMETIDINE	TABLET, FILM COATED	ORAL	20241112	N/A	ANDA	ANDA218997	Aurobindo Pharma Limited	CIMETIDINE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (59651-823-01)
59651-825-01	59651-825	HUMAN PRESCRIPTION DRUG	CIMETIDINE	CIMETIDINE	TABLET, FILM COATED	ORAL	20241112	N/A	ANDA	ANDA218997	Aurobindo Pharma Limited	CIMETIDINE	400 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (59651-825-01)
59651-825-05	59651-825	HUMAN PRESCRIPTION DRUG	CIMETIDINE	CIMETIDINE	TABLET, FILM COATED	ORAL	20241112	N/A	ANDA	ANDA218997	Aurobindo Pharma Limited	CIMETIDINE	400 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (59651-825-05)
59651-826-01	59651-826	HUMAN PRESCRIPTION DRUG	CIMETIDINE	CIMETIDINE	TABLET, FILM COATED	ORAL	20241112	N/A	ANDA	ANDA218997	Aurobindo Pharma Limited	CIMETIDINE	800 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (59651-826-01)
59651-824-01	59651-824	HUMAN PRESCRIPTION DRUG	CIMETIDINE	CIMETIDINE	TABLET, FILM COATED	ORAL	20241112	N/A	ANDA	ANDA218997	Aurobindo Pharma Limited	CIMETIDINE	300 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (59651-824-01)