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
51655-492-25	51655-492	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20220209	N/A	ANDA	ANDA090937	Northwind Pharmaceuticals, 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 Pharmaceuticals, 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 Pharmaceuticals, LLC	GLYBURIDE	5 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-492-52)
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)
68071-5217-0	68071-5217	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20200318	N/A	ANDA	ANDA090937	NuCare Pharmaceuticals,Inc.	GLYBURIDE	2.5 mg/1	100 TABLET in 1 BOTTLE (68071-5217-0)
23155-058-01	23155-058	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20101005	N/A	ANDA	ANDA090937	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	GLYBURIDE	5 mg/1	100 TABLET in 1 BOTTLE (23155-058-01)
23155-058-10	23155-058	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20101005	N/A	ANDA	ANDA090937	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	GLYBURIDE	5 mg/1	1000 TABLET in 1 BOTTLE (23155-058-10)
63187-659-30	63187-659	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20181201	N/A	ANDA	ANDA090937	Proficient Rx LP	GLYBURIDE	2.5 mg/1	30 TABLET in 1 BOTTLE (63187-659-30)
63187-659-60	63187-659	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20181201	N/A	ANDA	ANDA090937	Proficient Rx LP	GLYBURIDE	2.5 mg/1	60 TABLET in 1 BOTTLE (63187-659-60)
63187-659-90	63187-659	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20181201	N/A	ANDA	ANDA090937	Proficient Rx LP	GLYBURIDE	2.5 mg/1	90 TABLET in 1 BOTTLE (63187-659-90)
68071-4695-3	68071-4695	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20190107	N/A	ANDA	ANDA090937	NuCare Pharmaceuticals,Inc.	GLYBURIDE	5 mg/1	30 TABLET in 1 BOTTLE (68071-4695-3)
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)
68071-5215-0	68071-5215	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20200318	N/A	ANDA	ANDA090937	NuCare Pharmaceuticals,Inc.	GLYBURIDE	5 mg/1	100 TABLET in 1 BOTTLE (68071-5215-0)
23155-057-01	23155-057	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20101005	N/A	ANDA	ANDA090937	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	GLYBURIDE	2.5 mg/1	100 TABLET in 1 BOTTLE (23155-057-01)
23155-057-10	23155-057	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20101005	N/A	ANDA	ANDA090937	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	GLYBURIDE	2.5 mg/1	1000 TABLET in 1 BOTTLE (23155-057-10)
68071-5030-0	68071-5030	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20190814	N/A	ANDA	ANDA090937	NuCare Pharmaceuticals,Inc.	GLYBURIDE	5 mg/1	100 TABLET in 1 BOTTLE (68071-5030-0)
53002-4170-3	53002-4170	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20200101	N/A	ANDA	ANDA090937	RPK Pharmaceuticals, Inc.	GLYBURIDE	5 mg/1	30 TABLET in 1 BOTTLE (53002-4170-3)
53002-4170-6	53002-4170	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20200101	N/A	ANDA	ANDA090937	RPK Pharmaceuticals, Inc.	GLYBURIDE	5 mg/1	60 TABLET in 1 BOTTLE (53002-4170-6)
53002-4170-0	53002-4170	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20200101	N/A	ANDA	ANDA090937	RPK Pharmaceuticals, Inc.	GLYBURIDE	5 mg/1	100 TABLET in 1 BOTTLE (53002-4170-0)
68071-4695-6	68071-4695	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20190107	N/A	ANDA	ANDA090937	NuCare Pharmaceuticals,Inc.	GLYBURIDE	5 mg/1	60 TABLET in 1 BOTTLE (68071-4695-6)