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
71335-0291-8	71335-0291	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20220628	N/A	ANDA	ANDA205119	Bryant Ranch Prepack	PANTOPRAZOLE SODIUM	20 mg/1	180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-8)
71335-0291-9	71335-0291	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20220628	N/A	ANDA	ANDA205119	Bryant Ranch Prepack	PANTOPRAZOLE SODIUM	20 mg/1	3 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-9)
71335-0291-2	71335-0291	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20220524	N/A	ANDA	ANDA205119	Bryant Ranch Prepack	PANTOPRAZOLE SODIUM	20 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-2)
71335-0291-3	71335-0291	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20220628	N/A	ANDA	ANDA205119	Bryant Ranch Prepack	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-3)
71335-0291-4	71335-0291	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium	Pantoprazole	TABLET, DELAYED RELEASE	ORAL	20220628	N/A	ANDA	ANDA205119	Bryant Ranch Prepack	PANTOPRAZOLE SODIUM	20 mg/1	56 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-4)
80425-0085-3	80425-0085	HUMAN PRESCRIPTION DRUG	Pantoprazole Sodium DR	Pantoprazole Sodium	TABLET, DELAYED RELEASE	ORAL	20160620	N/A	ANDA	ANDA205119	Advanced Rx of Tennessee, LLC	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0085-3)