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
51407-374-90	51407-374	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20200916	N/A	ANDA	ANDA078281	Golden State Medical Supply, Inc.	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (51407-374-90)
51407-250-90	51407-250	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20190530	N/A	ANDA	ANDA078281	Golden State Medical Supply, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (51407-250-90)
51407-250-10	51407-250	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20190530	N/A	ANDA	ANDA078281	Golden State Medical Supply, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (51407-250-10)
45865-785-30	45865-785	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20180601	N/A	ANDA	ANDA078281	medsource pharmaceuticals	PANTOPRAZOLE SODIUM	40 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (45865-785-30)
51407-612-90	51407-612	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20220127	N/A	ANDA	ANDA078281	Golden State Medical Supply, Inc.	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (51407-612-90)
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)
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)
50268-639-15	50268-639	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20150219	N/A	ANDA	ANDA078281	AvPAK	PANTOPRAZOLE SODIUM	40 mg/1	50 BLISTER PACK in 1 BOX (50268-639-15) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (50268-639-11)
53002-1419-3	53002-1419	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20170901	N/A	ANDA	ANDA078281	RPK Pharmaceuticals, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (53002-1419-3)
53002-1419-9	53002-1419	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20170901	N/A	ANDA	ANDA078281	RPK Pharmaceuticals, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (53002-1419-9)
62135-534-90	62135-534	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20230405	N/A	ANDA	ANDA078281	Chartwell RX, LLC	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (62135-534-90)
62135-533-90	62135-533	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20230405	N/A	ANDA	ANDA078281	Chartwell RX, LLC	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (62135-533-90)
62135-534-08	62135-534	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20230405	N/A	ANDA	ANDA078281	Chartwell RX, LLC	PANTOPRAZOLE SODIUM	40 mg/1	450 TABLET, DELAYED RELEASE in 1 BOTTLE (62135-534-08)
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)
62175-618-46	62175-618	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20110120	N/A	ANDA	ANDA078281	Lannett Company, Inc.	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-618-46)
63739-564-10	63739-564	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20110120	N/A	ANDA	ANDA078281	McKesson Corporation dba SKY Packaging	PANTOPRAZOLE SODIUM	40 mg/1	10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-564-10) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK
62175-617-43	62175-617	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20110120	N/A	ANDA	ANDA078281	Lannett Company, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-617-43)
62175-617-46	62175-617	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20110120	N/A	ANDA	ANDA078281	Lannett Company, Inc.	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-617-46)
62175-618-43	62175-618	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20110120	N/A	ANDA	ANDA078281	Lannett Company, Inc.	PANTOPRAZOLE SODIUM	20 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-618-43)