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
70756-019-90	70756-019	HUMAN PRESCRIPTION DRUG	Pantoprazole sodium delayed-release	Pantoprazole sodium delayed-release	TABLET	ORAL	20220727	N/A	ANDA	ANDA215880	Lifestar Pharma LLC	PANTOPRAZOLE SODIUM	40 mg/1	90 TABLET in 1 BOTTLE (70756-019-90)
70756-019-12	70756-019	HUMAN PRESCRIPTION DRUG	Pantoprazole sodium delayed-release	Pantoprazole sodium delayed-release	TABLET	ORAL	20220727	N/A	ANDA	ANDA215880	Lifestar Pharma LLC	PANTOPRAZOLE SODIUM	40 mg/1	1000 TABLET in 1 BOTTLE (70756-019-12)
70756-018-90	70756-018	HUMAN PRESCRIPTION DRUG	Pantoprazole sodium delayed-release	Pantoprazole sodium delayed-release	TABLET	ORAL	20240425	N/A	ANDA	ANDA215880	Lifestar Pharma LLC	PANTOPRAZOLE SODIUM	20 mg/1	90 TABLET in 1 BOTTLE (70756-018-90)
70756-018-51	70756-018	HUMAN PRESCRIPTION DRUG	Pantoprazole sodium delayed-release	Pantoprazole sodium delayed-release	TABLET	ORAL	20240425	N/A	ANDA	ANDA215880	Lifestar Pharma LLC	PANTOPRAZOLE SODIUM	20 mg/1	500 TABLET in 1 BOTTLE (70756-018-51)