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
42571-101-01	42571-101	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20130613	N/A	ANDA	ANDA091220	Micro Labs Limited	GLIMEPIRIDE	2 mg/1	100 TABLET in 1 BOTTLE (42571-101-01)
42571-100-05	42571-100	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20130613	N/A	ANDA	ANDA091220	Micro Labs Limited	GLIMEPIRIDE	1 mg/1	500 TABLET in 1 BOTTLE (42571-100-05)
42571-100-01	42571-100	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20130613	N/A	ANDA	ANDA091220	Micro Labs Limited	GLIMEPIRIDE	1 mg/1	100 TABLET in 1 BOTTLE (42571-100-01)
72336-641-01	72336-641	HUMAN PRESCRIPTION DRUG	Glimepiride 3 mg	Glimepiride	TABLET	ORAL	20240820	N/A	ANDA	ANDA091220	Lifsa Drugs LLC	GLIMEPIRIDE	3 mg/1	100 TABLET in 1 BOTTLE (72336-641-01)
0615-8334-39	0615-8334	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20200413	N/A	ANDA	ANDA091220	NCS HealthCare of KY, Inc dba Vangard Labs	GLIMEPIRIDE	4 mg/1	30 TABLET in 1 BLISTER PACK (0615-8334-39)
0615-8333-39	0615-8333	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20200413	N/A	ANDA	ANDA091220	NCS HealthCare of KY, Inc dba Vangard Labs	GLIMEPIRIDE	2 mg/1	30 TABLET in 1 BLISTER PACK (0615-8333-39)
0615-8332-39	0615-8332	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20200410	N/A	ANDA	ANDA091220	NCS HealthCare of KY, Inc dba Vangard Labs	GLIMEPIRIDE	1 mg/1	30 TABLET in 1 BLISTER PACK (0615-8332-39)