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
70518-3829-1	70518-3829	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20231106	N/A	ANDA	ANDA215630	REMEDYREPACK INC.	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-1)
70518-3829-2	70518-3829	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20231223	N/A	ANDA	ANDA215630	REMEDYREPACK INC.	FAMOTIDINE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-2)
70518-3829-3	70518-3829	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20240124	N/A	ANDA	ANDA215630	REMEDYREPACK INC.	FAMOTIDINE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-3)
70518-3829-4	70518-3829	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20240228	N/A	ANDA	ANDA215630	REMEDYREPACK INC.	FAMOTIDINE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-4)
70518-3829-5	70518-3829	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20240612	N/A	ANDA	ANDA215630	REMEDYREPACK INC.	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3829-5)
70518-3831-0	70518-3831	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20230816	N/A	ANDA	ANDA215630	REMEDYREPACK INC.	FAMOTIDINE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3831-0)
70518-3831-1	70518-3831	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20231004	N/A	ANDA	ANDA215630	REMEDYREPACK INC.	FAMOTIDINE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3831-1)
70518-3831-2	70518-3831	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20240126	N/A	ANDA	ANDA215630	REMEDYREPACK INC.	FAMOTIDINE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3831-2)
70518-4084-0	70518-4084	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20240517	N/A	ANDA	ANDA215630	REMEDYREPACK INC.	FAMOTIDINE	40 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4084-0)
60760-843-07	60760-843	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20230620	N/A	ANDA	ANDA215630	ST. MARY'S MEDICAL PARK PHARMACY	FAMOTIDINE	40 mg/1	7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-843-07)
60760-843-60	60760-843	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20230701	N/A	ANDA	ANDA215630	ST. MARY'S MEDICAL PARK PHARMACY	FAMOTIDINE	40 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-843-60)