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
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)
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)
0615-7629-28	0615-7629	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	pantoprazole sodium	TABLET, DELAYED RELEASE	ORAL	20240424	N/A	ANDA	ANDA090970	NCS HealthCare of KY, LLC dba Vangard Labs	PANTOPRAZOLE SODIUM	40 mg/1	28 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7629-28)
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)