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
76420-713-01	76420-713	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20240411	N/A	ANDA	ANDA215630	Asclemed USA, Inc.	FAMOTIDINE	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (76420-713-01)
76420-713-30	76420-713	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20240411	N/A	ANDA	ANDA215630	Asclemed USA, Inc.	FAMOTIDINE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-713-30)
67877-842-01	67877-842	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20220708	N/A	ANDA	ANDA215630	Ascend Laboratories, LLC	FAMOTIDINE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (67877-842-01)
67877-842-05	67877-842	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20250203	N/A	ANDA	ANDA215630	Ascend Laboratories, LLC	FAMOTIDINE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (67877-842-05)
67877-842-10	67877-842	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20220708	N/A	ANDA	ANDA215630	Ascend Laboratories, LLC	FAMOTIDINE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (67877-842-10)
50090-6582-1	50090-6582	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20230809	N/A	ANDA	ANDA215630	A-S Medication Solutions	FAMOTIDINE	20 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (50090-6582-1)
50090-6582-2	50090-6582	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20230809	N/A	ANDA	ANDA215630	A-S Medication Solutions	FAMOTIDINE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (50090-6582-2)
50090-6582-3	50090-6582	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20230809	N/A	ANDA	ANDA215630	A-S Medication Solutions	FAMOTIDINE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-6582-3)
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)
70518-3829-6	70518-3829	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20241121	N/A	ANDA	ANDA215630	REMEDYREPACK INC.	FAMOTIDINE	20 mg/1	14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-6)
68788-8485-3	68788-8485	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20230718	N/A	ANDA	ANDA215630	Preferred Pharmaceuticals Inc.	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-8485-3)
68788-8485-4	68788-8485	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20230718	N/A	ANDA	ANDA215630	Preferred Pharmaceuticals Inc.	FAMOTIDINE	20 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (68788-8485-4)
68788-8485-6	68788-8485	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20230718	N/A	ANDA	ANDA215630	Preferred Pharmaceuticals Inc.	FAMOTIDINE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-8485-6)
68788-8485-9	68788-8485	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20230718	N/A	ANDA	ANDA215630	Preferred Pharmaceuticals Inc.	FAMOTIDINE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-8485-9)