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
72162-2503-3	72162-2503	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	rabeprazole sodium	TABLET, DELAYED RELEASE	ORAL	20250513	N/A	ANDA	ANDA204237	Bryant Ranch Prepack	RABEPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2503-3)
72162-2503-5	72162-2503	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	rabeprazole sodium	TABLET, DELAYED RELEASE	ORAL	20250513	N/A	ANDA	ANDA204237	Bryant Ranch Prepack	RABEPRAZOLE SODIUM	20 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2503-5)
72162-2503-9	72162-2503	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	rabeprazole sodium	TABLET, DELAYED RELEASE	ORAL	20250513	N/A	ANDA	ANDA204237	Bryant Ranch Prepack	RABEPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2503-9)
72888-059-90	72888-059	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	rabeprazole sodium	TABLET, DELAYED RELEASE	ORAL	20170601	N/A	ANDA	ANDA204237	Advagen Pharma Limited	RABEPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (72888-059-90)
76420-223-30	76420-223	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	rabeprazole sodium	TABLET, DELAYED RELEASE	ORAL	20220707	N/A	ANDA	ANDA204237	Asclemed USA, Inc.	RABEPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-223-30)
76420-223-60	76420-223	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	rabeprazole sodium	TABLET, DELAYED RELEASE	ORAL	20220707	N/A	ANDA	ANDA204237	Asclemed USA, Inc.	RABEPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-223-60)
76420-223-90	76420-223	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	rabeprazole sodium	TABLET, DELAYED RELEASE	ORAL	20220707	N/A	ANDA	ANDA204237	Asclemed USA, Inc.	RABEPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-223-90)
72888-059-30	72888-059	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	rabeprazole sodium	TABLET, DELAYED RELEASE	ORAL	20170601	N/A	ANDA	ANDA204237	Advagen Pharma Limited	RABEPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (72888-059-30)
60760-972-07	60760-972	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	rabeprazole sodium	TABLET, DELAYED RELEASE	ORAL	20240319	N/A	ANDA	ANDA204237	St. Mary's Medical Park Pharmacy	RABEPRAZOLE SODIUM	20 mg/1	7 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-972-07)
60760-972-30	60760-972	HUMAN PRESCRIPTION DRUG	RABEPRAZOLE SODIUM	rabeprazole sodium	TABLET, DELAYED RELEASE	ORAL	20210506	N/A	ANDA	ANDA204237	St. Mary's Medical Park Pharmacy	RABEPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-972-30)