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
23155-056-10	23155-056	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20101005	N/A	ANDA	ANDA090937	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	GLYBURIDE	1.25 mg/1	1000 TABLET in 1 BOTTLE (23155-056-10)
51655-492-25	51655-492	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20220209	N/A	ANDA	ANDA090937	Northwind Health Company, LLC	GLYBURIDE	5 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (51655-492-25)
51655-492-26	51655-492	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20231116	N/A	ANDA	ANDA090937	Northwind Health Company, LLC	GLYBURIDE	5 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (51655-492-26)
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)
71335-0150-6	71335-0150	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20210212	N/A	ANDA	ANDA090937	Bryant Ranch Prepack	GLYBURIDE	5 mg/1	180 TABLET in 1 BOTTLE (71335-0150-6)