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
51655-492-52	51655-492	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20210107	N/A	ANDA	ANDA090937	Northwind Health Company, LLC	GLYBURIDE	5 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-492-52)
51655-659-52	51655-659	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20210323	N/A	ANDA	ANDA090937	Northwind Health Company, LLC	GLYBURIDE	2.5 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-659-52)
62135-583-30	62135-583	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20230509	N/A	ANDA	ANDA090937	Chartwell RX, LLC	GLYBURIDE	1.25 mg/1	30 TABLET in 1 BOTTLE (62135-583-30)
62135-584-30	62135-584	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20230509	N/A	ANDA	ANDA090937	Chartwell RX, LLC	GLYBURIDE	2.5 mg/1	30 TABLET in 1 BOTTLE (62135-584-30)
62135-585-90	62135-585	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20230509	N/A	ANDA	ANDA090937	Chartwell RX, LLC	GLYBURIDE	5 mg/1	90 TABLET in 1 BOTTLE (62135-585-90)