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
60760-574-30	60760-574	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20230829	N/A	ANDA	ANDA077619	ST. MARY'S MEDICAL PARK PHARMACY	PANTOPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-574-30)
60760-574-60	60760-574	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20221031	N/A	ANDA	ANDA077619	ST. MARY'S MEDICAL PARK PHARMACY	PANTOPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-574-60)
70518-4060-0	70518-4060	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20240502	N/A	ANDA	ANDA077619	REMEDYREPACK INC.	PANTOPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-4060-0)
68788-8505-6	68788-8505	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20230815	N/A	ANDA	ANDA077619	Preferred Pharmaceuticals Inc.	PANTOPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8505-6)
68788-8505-9	68788-8505	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20230815	N/A	ANDA	ANDA077619	Preferred Pharmaceuticals Inc.	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8505-9)
68788-8505-3	68788-8505	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20230815	N/A	ANDA	ANDA077619	Preferred Pharmaceuticals Inc.	PANTOPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8505-3)
68788-8505-1	68788-8505	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20230815	N/A	ANDA	ANDA077619	Preferred Pharmaceuticals Inc.	PANTOPRAZOLE SODIUM	20 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8505-1)
68788-8505-8	68788-8505	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20230815	N/A	ANDA	ANDA077619	Preferred Pharmaceuticals Inc.	PANTOPRAZOLE SODIUM	20 mg/1	120 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8505-8)
68071-2891-3	68071-2891	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20230105	N/A	ANDA	ANDA077619	NuCare Pharmaceuticals,Inc.	PANTOPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-2891-3)
68071-2891-6	68071-2891	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20221130	N/A	ANDA	ANDA077619	NuCare Pharmaceuticals,Inc.	PANTOPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-2891-6)
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)
72603-178-01	72603-178	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20231215	N/A	ANDA	ANDA077619	NorthStar RxLLC	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (72603-178-01)
68071-2845-9	68071-2845	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20221005	N/A	ANDA	ANDA077619	NuCare Pharmaceuticals,Inc.	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-2845-9)
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)
55111-332-01	55111-332	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20110119	N/A	ANDA	ANDA077619	Dr.Reddy's Laboratories Limited	PANTOPRAZOLE SODIUM	20 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-332-01)
55111-332-78	55111-332	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20110119	N/A	ANDA	ANDA077619	Dr.Reddy's Laboratories Limited	PANTOPRAZOLE SODIUM	20 mg/1	10 BLISTER PACK in 1 CARTON (55111-332-78) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-332-79)
55111-332-81	55111-332	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20110119	N/A	ANDA	ANDA077619	Dr.Reddy's Laboratories Limited	PANTOPRAZOLE SODIUM	20 mg/1	3 BLISTER PACK in 1 CARTON (55111-332-81) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-332-79)
55111-332-90	55111-332	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20110119	N/A	ANDA	ANDA077619	Dr.Reddy's Laboratories Limited	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-332-90)
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)