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
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)
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)
63187-667-30	63187-667	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20181201	N/A	ANDA	ANDA090937	Proficient Rx LP	GLYBURIDE	5 mg/1	30 TABLET in 1 BOTTLE (63187-667-30)
63187-667-60	63187-667	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20181201	N/A	ANDA	ANDA090937	Proficient Rx LP	GLYBURIDE	5 mg/1	60 TABLET in 1 BOTTLE (63187-667-60)
63187-667-90	63187-667	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20181201	N/A	ANDA	ANDA090937	Proficient Rx LP	GLYBURIDE	5 mg/1	90 TABLET in 1 BOTTLE (63187-667-90)
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)
23155-056-01	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	100 TABLET in 1 BOTTLE (23155-056-01)
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)
51655-659-52	51655-659	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20210323	N/A	ANDA	ANDA090937	Northwind Pharmaceuticals	GLYBURIDE	2.5 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-659-52)
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)
71335-0150-1	71335-0150	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20180904	N/A	ANDA	ANDA090937	Bryant Ranch Prepack	GLYBURIDE	5 mg/1	30 TABLET in 1 BOTTLE (71335-0150-1)
71335-0150-2	71335-0150	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20250128	N/A	ANDA	ANDA090937	Bryant Ranch Prepack	GLYBURIDE	5 mg/1	120 TABLET in 1 BOTTLE (71335-0150-2)
71335-0150-3	71335-0150	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20250128	N/A	ANDA	ANDA090937	Bryant Ranch Prepack	GLYBURIDE	5 mg/1	100 TABLET in 1 BOTTLE (71335-0150-3)
71335-0150-4	71335-0150	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20180723	N/A	ANDA	ANDA090937	Bryant Ranch Prepack	GLYBURIDE	5 mg/1	60 TABLET in 1 BOTTLE (71335-0150-4)
71335-0150-5	71335-0150	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20180523	N/A	ANDA	ANDA090937	Bryant Ranch Prepack	GLYBURIDE	5 mg/1	90 TABLET in 1 BOTTLE (71335-0150-5)