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
72603-177-01	72603-177	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20231215	N/A	ANDA	ANDA077619	NorthStar RxLLC	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (72603-177-01)
68071-3524-3	68071-3524	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20231018	N/A	ANDA	ANDA077619	NuCare Pharmaceuticals,Inc.	PANTOPRAZOLE SODIUM	40 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3524-3)
85509-1332-3	85509-1332	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20251120	N/A	ANDA	ANDA077619	PHOENIX RX LLC	PANTOPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1332-3)
85509-1332-6	85509-1332	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20251120	N/A	ANDA	ANDA077619	PHOENIX RX LLC	PANTOPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1332-6)
85509-1332-9	85509-1332	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20251120	N/A	ANDA	ANDA077619	PHOENIX RX LLC	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1332-9)
55111-333-01	55111-333	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20110119	N/A	ANDA	ANDA077619	Dr.Reddy's Laboratories Limited	PANTOPRAZOLE SODIUM	40 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-01)
55111-333-05	55111-333	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20110119	N/A	ANDA	ANDA077619	Dr.Reddy's Laboratories Limited	PANTOPRAZOLE SODIUM	40 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-05)
55111-333-10	55111-333	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20110119	N/A	ANDA	ANDA077619	Dr.Reddy's Laboratories Limited	PANTOPRAZOLE SODIUM	40 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-10)
55111-333-30	55111-333	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20110119	N/A	ANDA	ANDA077619	Dr.Reddy's Laboratories Limited	PANTOPRAZOLE SODIUM	40 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-30)
55111-333-78	55111-333	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20110119	N/A	ANDA	ANDA077619	Dr.Reddy's Laboratories Limited	PANTOPRAZOLE SODIUM	40 mg/1	10 BLISTER PACK in 1 CARTON (55111-333-78) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-333-79)
55111-333-81	55111-333	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20110119	N/A	ANDA	ANDA077619	Dr.Reddy's Laboratories Limited	PANTOPRAZOLE SODIUM	40 mg/1	3 BLISTER PACK in 1 CARTON (55111-333-81) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-333-79)
55111-333-90	55111-333	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20110119	N/A	ANDA	ANDA077619	Dr.Reddy's Laboratories Limited	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-90)