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
61919-250-04	61919-250	HUMAN PRESCRIPTION DRUG	GLIMEPIRIDE	GLIMEPIRIDE	TABLET	ORAL	20160204	N/A	ANDA	ANDA078181	DIRECT RX	GLIMEPIRIDE	4 mg/1	4 TABLET in 1 BOTTLE (61919-250-04)
61919-250-30	61919-250	HUMAN PRESCRIPTION DRUG	GLIMEPIRIDE	GLIMEPIRIDE	TABLET	ORAL	20160204	N/A	ANDA	ANDA078181	DIRECT RX	GLIMEPIRIDE	4 mg/1	30 TABLET in 1 BOTTLE (61919-250-30)
61919-250-60	61919-250	HUMAN PRESCRIPTION DRUG	GLIMEPIRIDE	GLIMEPIRIDE	TABLET	ORAL	20160204	N/A	ANDA	ANDA078181	DIRECT RX	GLIMEPIRIDE	4 mg/1	60 TABLET in 1 BOTTLE (61919-250-60)
61919-250-82	61919-250	HUMAN PRESCRIPTION DRUG	GLIMEPIRIDE	GLIMEPIRIDE	TABLET	ORAL	20160204	N/A	ANDA	ANDA078181	DIRECT RX	GLIMEPIRIDE	4 mg/1	180 TABLET in 1 BOTTLE (61919-250-82)
61919-250-90	61919-250	HUMAN PRESCRIPTION DRUG	GLIMEPIRIDE	GLIMEPIRIDE	TABLET	ORAL	20160204	N/A	ANDA	ANDA078181	DIRECT RX	GLIMEPIRIDE	4 mg/1	90 TABLET in 1 BOTTLE (61919-250-90)
51655-120-26	51655-120	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20221206	N/A	ANDA	ANDA078181	Northwind Pharmaceuticals, LLC	GLIMEPIRIDE	4 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (51655-120-26)
51655-120-52	51655-120	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20141229	N/A	ANDA	ANDA078181	Northwind Pharmaceuticals, LLC	GLIMEPIRIDE	4 mg/1	30 TABLET in 1 BOTTLE, DISPENSING (51655-120-52)