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
43353-027-80	43353-027	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20160419	N/A	ANDA	ANDA078281	Aphena Pharma Solutions - Tennessee, LLC	PANTOPRAZOLE SODIUM	40 mg/1	180 TABLET, DELAYED RELEASE in 1 BOTTLE (43353-027-80)
51407-613-10	51407-613	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20220127	N/A	ANDA	ANDA078281	Golden State Medical Supply, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (51407-613-10)
51407-613-90	51407-613	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20220127	N/A	ANDA	ANDA078281	Golden State Medical Supply, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (51407-613-90)
72789-086-30	72789-086	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20200604	N/A	ANDA	ANDA078281	PD-Rx Pharmaceuticals, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-086-30)
50268-585-15	50268-585	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20210128	N/A	ANDA	ANDA078281	AvPAK	PANTOPRAZOLE SODIUM	20 mg/1	50 BLISTER PACK in 1 BOX (50268-585-15) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (50268-585-11)