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
60760-800-90	60760-800	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20230519	N/A	ANDA	ANDA202759	ST. MARY'S MEDICAL PARK PHARMACY	GLIMEPIRIDE	4 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (60760-800-90)
50090-6426-0	50090-6426	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20230407	N/A	ANDA	ANDA202759	A-S Medication Solutions	GLIMEPIRIDE	2 mg/1	30 TABLET in 1 BOTTLE (50090-6426-0)
50090-6426-1	50090-6426	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20230407	N/A	ANDA	ANDA202759	A-S Medication Solutions	GLIMEPIRIDE	2 mg/1	100 TABLET in 1 BOTTLE (50090-6426-1)
50090-6426-3	50090-6426	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20230407	N/A	ANDA	ANDA202759	A-S Medication Solutions	GLIMEPIRIDE	2 mg/1	90 TABLET in 1 BOTTLE (50090-6426-3)
50090-6426-4	50090-6426	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20230407	N/A	ANDA	ANDA202759	A-S Medication Solutions	GLIMEPIRIDE	2 mg/1	180 TABLET in 1 BOTTLE (50090-6426-4)
16571-773-01	16571-773	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20120629	N/A	ANDA	ANDA202759	Rising Pharma Holdings, Inc.	GLIMEPIRIDE	1 mg/1	100 TABLET in 1 BOTTLE (16571-773-01)
16571-773-50	16571-773	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20120629	N/A	ANDA	ANDA202759	Rising Pharma Holdings, Inc.	GLIMEPIRIDE	1 mg/1	500 TABLET in 1 BOTTLE (16571-773-50)
71205-773-30	71205-773	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20230313	N/A	ANDA	ANDA202759	Proficient Rx LP	GLIMEPIRIDE	4 mg/1	30 TABLET in 1 BOTTLE (71205-773-30)
71205-773-60	71205-773	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20230313	N/A	ANDA	ANDA202759	Proficient Rx LP	GLIMEPIRIDE	4 mg/1	60 TABLET in 1 BOTTLE (71205-773-60)
71205-773-78	71205-773	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20230313	N/A	ANDA	ANDA202759	Proficient Rx LP	GLIMEPIRIDE	4 mg/1	180 TABLET in 1 BOTTLE (71205-773-78)
71205-773-90	71205-773	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20230313	N/A	ANDA	ANDA202759	Proficient Rx LP	GLIMEPIRIDE	4 mg/1	90 TABLET in 1 BOTTLE (71205-773-90)
50090-7628-0	50090-7628	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20250811	N/A	ANDA	ANDA202759	A-S Medication Solutions	GLIMEPIRIDE	2 mg/1	90 TABLET in 1 BOTTLE (50090-7628-0)
16571-774-01	16571-774	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20120629	N/A	ANDA	ANDA202759	Rising Pharma Holdings, Inc.	GLIMEPIRIDE	2 mg/1	100 TABLET in 1 BOTTLE (16571-774-01)
16571-774-50	16571-774	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20120629	N/A	ANDA	ANDA202759	Rising Pharma Holdings, Inc.	GLIMEPIRIDE	2 mg/1	500 TABLET in 1 BOTTLE (16571-774-50)
71205-779-30	71205-779	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20230323	N/A	ANDA	ANDA202759	Proficient Rx LP	GLIMEPIRIDE	1 mg/1	30 TABLET in 1 BOTTLE (71205-779-30)
71205-779-60	71205-779	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20230323	N/A	ANDA	ANDA202759	Proficient Rx LP	GLIMEPIRIDE	1 mg/1	60 TABLET in 1 BOTTLE (71205-779-60)
71205-779-90	71205-779	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20230323	N/A	ANDA	ANDA202759	Proficient Rx LP	GLIMEPIRIDE	1 mg/1	90 TABLET in 1 BOTTLE (71205-779-90)
65862-580-01	65862-580	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20120629	N/A	ANDA	ANDA202759	Aurobindo Pharma Limited	GLIMEPIRIDE	2 mg/1	100 TABLET in 1 BOTTLE (65862-580-01)
65862-580-05	65862-580	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20120629	N/A	ANDA	ANDA202759	Aurobindo Pharma Limited	GLIMEPIRIDE	2 mg/1	500 TABLET in 1 BOTTLE (65862-580-05)
65862-580-99	65862-580	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20120629	N/A	ANDA	ANDA202759	Aurobindo Pharma Limited	GLIMEPIRIDE	2 mg/1	1000 TABLET in 1 BOTTLE (65862-580-99)