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
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)
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)
80425-0552-1	80425-0552	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20251015	N/A	ANDA	ANDA077619	Advanced Rx of Tennessee, LLC	PANTOPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0552-1)
80425-0552-2	80425-0552	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20251015	N/A	ANDA	ANDA077619	Advanced Rx of Tennessee, LLC	PANTOPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0552-2)
80425-0552-3	80425-0552	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20251015	N/A	ANDA	ANDA077619	Advanced Rx of Tennessee, LLC	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0552-3)
68071-3776-3	68071-3776	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20250129	N/A	ANDA	ANDA077619	NuCare Pharmaceuticals, Inc.	PANTOPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3776-3)
68071-3776-6	68071-3776	HUMAN PRESCRIPTION DRUG	Pantoprazole	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20250117	N/A	ANDA	ANDA077619	NuCare Pharmaceuticals, Inc.	PANTOPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3776-6)
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)
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)
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)