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
72241-040-10	72241-040	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20211005	N/A	ANDA	ANDA203379	Modavar Pharmaceuticals LLC	GLYBURIDE	5 mg/1	500 TABLET in 1 BOTTLE (72241-040-10)
72241-040-11	72241-040	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20211005	N/A	ANDA	ANDA203379	Modavar Pharmaceuticals LLC	GLYBURIDE	5 mg/1	1000 TABLET in 1 BOTTLE (72241-040-11)
67046-1345-3	67046-1345	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20241111	N/A	ANDA	ANDA203379	Coupler LLC	GLYBURIDE	2.5 mg/1	30 TABLET in 1 BLISTER PACK (67046-1345-3)
68071-3492-0	68071-3492	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20230825	N/A	ANDA	ANDA203379	NuCare Pharmaceuticals,Inc.	GLYBURIDE	2.5 mg/1	100 TABLET in 1 BOTTLE (68071-3492-0)
75834-203-00	75834-203	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20190125	N/A	ANDA	ANDA203379	Nivagen Pharmaceuticals, Inc.	GLYBURIDE	2.5 mg/1	1000 TABLET in 1 BOTTLE (75834-203-00)
75834-203-01	75834-203	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20190125	N/A	ANDA	ANDA203379	Nivagen Pharmaceuticals, Inc.	GLYBURIDE	2.5 mg/1	100 TABLET in 1 BOTTLE (75834-203-01)
70518-3504-0	70518-3504	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20220831	N/A	ANDA	ANDA203379	REMEDYREPACK INC.	GLYBURIDE	2.5 mg/1	30 TABLET in 1 BLISTER PACK (70518-3504-0)
70518-3504-1	70518-3504	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20240212	N/A	ANDA	ANDA203379	REMEDYREPACK INC.	GLYBURIDE	2.5 mg/1	30 TABLET in 1 BLISTER PACK (70518-3504-1)
72241-039-05	72241-039	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20211005	N/A	ANDA	ANDA203379	Modavar Pharmaceuticals LLC	GLYBURIDE	2.5 mg/1	100 TABLET in 1 BOTTLE (72241-039-05)
72241-039-10	72241-039	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20211005	N/A	ANDA	ANDA203379	Modavar Pharmaceuticals LLC	GLYBURIDE	2.5 mg/1	500 TABLET in 1 BOTTLE (72241-039-10)
72241-039-11	72241-039	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20211005	N/A	ANDA	ANDA203379	Modavar Pharmaceuticals LLC	GLYBURIDE	2.5 mg/1	1000 TABLET in 1 BOTTLE (72241-039-11)
71209-011-05	71209-011	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20140426	N/A	ANDA	ANDA203379	Cadila Pharmaceuticals Limited	GLYBURIDE	5 mg/1	100 TABLET in 1 BOTTLE (71209-011-05)
71209-011-10	71209-011	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20190820	N/A	ANDA	ANDA203379	Cadila Pharmaceuticals Limited	GLYBURIDE	5 mg/1	500 TABLET in 1 BOTTLE (71209-011-10)
71209-011-11	71209-011	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20140426	N/A	ANDA	ANDA203379	Cadila Pharmaceuticals Limited	GLYBURIDE	5 mg/1	1000 TABLET in 1 BOTTLE (71209-011-11)
68071-3452-3	68071-3452	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20230706	N/A	ANDA	ANDA203379	NuCare Pharmaceuticals,Inc.	GLYBURIDE	5 mg/1	30 TABLET in 1 BOTTLE (68071-3452-3)
75834-202-00	75834-202	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20190125	N/A	ANDA	ANDA203379	Nivagen Pharmaceuticals, Inc.	GLYBURIDE	1.25 mg/1	1000 TABLET in 1 BOTTLE (75834-202-00)
75834-202-01	75834-202	HUMAN PRESCRIPTION DRUG	GLYBURIDE	GLYBURIDE	TABLET	ORAL	20190125	N/A	ANDA	ANDA203379	Nivagen Pharmaceuticals, Inc.	GLYBURIDE	1.25 mg/1	100 TABLET in 1 BOTTLE (75834-202-01)
68788-8508-1	68788-8508	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20230816	N/A	ANDA	ANDA203379	Preferred Pharmaceuticals Inc.	GLYBURIDE	5 mg/1	100 TABLET in 1 BOTTLE (68788-8508-1)
68788-8508-3	68788-8508	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20230816	N/A	ANDA	ANDA203379	Preferred Pharmaceuticals Inc.	GLYBURIDE	5 mg/1	30 TABLET in 1 BOTTLE (68788-8508-3)
68788-8508-6	68788-8508	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20230816	N/A	ANDA	ANDA203379	Preferred Pharmaceuticals Inc.	GLYBURIDE	5 mg/1	60 TABLET in 1 BOTTLE (68788-8508-6)