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
50090-6196-0	50090-6196	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20221031	N/A	ANDA	ANDA203379	A-S Medication Solutions	GLYBURIDE	5 mg/1	30 TABLET in 1 BOTTLE (50090-6196-0)
50090-6196-1	50090-6196	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20221104	N/A	ANDA	ANDA203379	A-S Medication Solutions	GLYBURIDE	5 mg/1	100 TABLET in 1 BOTTLE (50090-6196-1)
50090-6196-2	50090-6196	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20221031	N/A	ANDA	ANDA203379	A-S Medication Solutions	GLYBURIDE	5 mg/1	60 TABLET in 1 BOTTLE (50090-6196-2)
50090-6196-8	50090-6196	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20221104	N/A	ANDA	ANDA203379	A-S Medication Solutions	GLYBURIDE	5 mg/1	200 TABLET in 1 BOTTLE (50090-6196-8)
50090-6196-9	50090-6196	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20221104	N/A	ANDA	ANDA203379	A-S Medication Solutions	GLYBURIDE	5 mg/1	90 TABLET in 1 BOTTLE (50090-6196-9)
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)
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)
68071-3492-0	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)
72241-038-05	72241-038	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20211005	N/A	ANDA	ANDA203379	Modavar Pharmaceuticals LLC	GLYBURIDE	1.25 mg/1	100 TABLET in 1 BOTTLE (72241-038-05)
72241-038-11	72241-038	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20211005	N/A	ANDA	ANDA203379	Modavar Pharmaceuticals LLC	GLYBURIDE	1.25 mg/1	1000 TABLET in 1 BOTTLE (72241-038-11)
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)
71209-010-05	71209-010	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20140426	N/A	ANDA	ANDA203379	Cadila Pharmaceuticals Limited	GLYBURIDE	2.5 mg/1	100 TABLET in 1 BOTTLE (71209-010-05)
71209-010-10	71209-010	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20190820	N/A	ANDA	ANDA203379	Cadila Pharmaceuticals Limited	GLYBURIDE	2.5 mg/1	500 TABLET in 1 BOTTLE (71209-010-10)
71209-010-11	71209-010	HUMAN PRESCRIPTION DRUG	Glyburide	Glyburide	TABLET	ORAL	20140426	N/A	ANDA	ANDA203379	Cadila Pharmaceuticals Limited	GLYBURIDE	2.5 mg/1	1000 TABLET in 1 BOTTLE (71209-010-11)
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)