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
42708-180-30	42708-180	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	pantoprazole sodium	TABLET, DELAYED RELEASE	ORAL	20230519	N/A	ANDA	ANDA090970	QPharma Inc	PANTOPRAZOLE SODIUM	40 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (42708-180-30)
55154-4382-0	55154-4382	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	pantoprazole sodium	TABLET, DELAYED RELEASE	ORAL	20110223	N/A	ANDA	ANDA090970	Cardinal Health 107, LLC	PANTOPRAZOLE SODIUM	40 mg/1	10 BLISTER PACK in 1 BAG (55154-4382-0) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
51079-051-20	51079-051	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	pantoprazole sodium	TABLET, DELAYED RELEASE	ORAL	20110223	N/A	ANDA	ANDA090970	Mylan Institutional Inc.	PANTOPRAZOLE SODIUM	40 mg/1	100 BLISTER PACK in 1 CARTON (51079-051-20) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (51079-051-01)
80425-0179-2	80425-0179	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium DR	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20110119	N/A	ANDA	ANDA090970	Advanced Rx Pharmacy of Tennessee, LLC	PANTOPRAZOLE SODIUM	20 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0179-2)
80425-0179-3	80425-0179	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium DR	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20110119	N/A	ANDA	ANDA090970	Advanced Rx Pharmacy of Tennessee, LLC	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0179-3)
67296-2047-3	67296-2047	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	pantoprazole sodium	TABLET, DELAYED RELEASE	ORAL	20110119	N/A	ANDA	ANDA090970	Redpharm drug	PANTOPRAZOLE SODIUM	40 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (67296-2047-3)
0615-7629-05	0615-7629	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	pantoprazole sodium	TABLET, DELAYED RELEASE	ORAL	20220406	N/A	ANDA	ANDA090970	NCS HealthCare of KY, LLC dba Vangard Labs	PANTOPRAZOLE SODIUM	40 mg/1	15 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7629-05)
0615-7629-07	0615-7629	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	pantoprazole sodium	TABLET, DELAYED RELEASE	ORAL	20220406	N/A	ANDA	ANDA090970	NCS HealthCare of KY, LLC dba Vangard Labs	PANTOPRAZOLE SODIUM	40 mg/1	7 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7629-07)
0615-7629-14	0615-7629	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	pantoprazole sodium	TABLET, DELAYED RELEASE	ORAL	20220406	N/A	ANDA	ANDA090970	NCS HealthCare of KY, LLC dba Vangard Labs	PANTOPRAZOLE SODIUM	40 mg/1	14 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7629-14)
0615-7629-30	0615-7629	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	pantoprazole sodium	TABLET, DELAYED RELEASE	ORAL	20220411	N/A	ANDA	ANDA090970	NCS HealthCare of KY, LLC dba Vangard Labs	PANTOPRAZOLE SODIUM	40 mg/1	6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-7629-30) / 5 TABLET, DELAYED RELEASE in 1 BLISTER PACK
0615-7629-39	0615-7629	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	pantoprazole sodium	TABLET, DELAYED RELEASE	ORAL	20220406	N/A	ANDA	ANDA090970	NCS HealthCare of KY, LLC dba Vangard Labs	PANTOPRAZOLE SODIUM	40 mg/1	30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7629-39)
0378-6688-77	0378-6688	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	pantoprazole sodium	TABLET, DELAYED RELEASE	ORAL	20110119	N/A	ANDA	ANDA090970	Mylan Pharmaceuticals Inc.	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (0378-6688-77)
0378-6689-10	0378-6689	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	pantoprazole sodium	TABLET, DELAYED RELEASE	ORAL	20110119	N/A	ANDA	ANDA090970	Mylan Pharmaceuticals Inc.	PANTOPRAZOLE SODIUM	40 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (0378-6689-10)
0378-6689-77	0378-6689	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	pantoprazole sodium	TABLET, DELAYED RELEASE	ORAL	20110119	N/A	ANDA	ANDA090970	Mylan Pharmaceuticals Inc.	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (0378-6689-77)