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
70518-3627-0	70518-3627	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20230129	N/A	ANDA	ANDA202759	REMEDYREPACK INC.	GLIMEPIRIDE	2 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70518-3627-0)
70518-3627-1	70518-3627	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20230209	N/A	ANDA	ANDA202759	REMEDYREPACK INC.	GLIMEPIRIDE	2 mg/1	30 TABLET in 1 BLISTER PACK (70518-3627-1)
70518-3627-2	70518-3627	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20230521	N/A	ANDA	ANDA202759	REMEDYREPACK INC.	GLIMEPIRIDE	2 mg/1	30 TABLET in 1 BLISTER PACK (70518-3627-2)
70518-3782-0	70518-3782	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20230711	N/A	ANDA	ANDA202759	REMEDYREPACK INC.	GLIMEPIRIDE	4 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70518-3782-0)
70518-3782-1	70518-3782	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20231031	N/A	ANDA	ANDA202759	REMEDYREPACK INC.	GLIMEPIRIDE	4 mg/1	30 TABLET in 1 BLISTER PACK (70518-3782-1)
70518-3782-2	70518-3782	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20240109	N/A	ANDA	ANDA202759	REMEDYREPACK INC.	GLIMEPIRIDE	4 mg/1	180 TABLET in 1 BOTTLE, PLASTIC (70518-3782-2)
70518-3782-3	70518-3782	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20240216	N/A	ANDA	ANDA202759	REMEDYREPACK INC.	GLIMEPIRIDE	4 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (70518-3782-3)
70518-3786-0	70518-3786	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20230711	N/A	ANDA	ANDA202759	REMEDYREPACK INC.	GLIMEPIRIDE	1 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70518-3786-0)
70518-3786-1	70518-3786	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20231226	N/A	ANDA	ANDA202759	REMEDYREPACK INC.	GLIMEPIRIDE	1 mg/1	180 TABLET in 1 BOTTLE, PLASTIC (70518-3786-1)
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)
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)
16571-775-01	16571-775	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20120629	N/A	ANDA	ANDA202759	Rising Pharma Holdings, Inc.	GLIMEPIRIDE	4 mg/1	100 TABLET in 1 BOTTLE (16571-775-01)
16571-775-50	16571-775	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20120629	N/A	ANDA	ANDA202759	Rising Pharma Holdings, Inc.	GLIMEPIRIDE	4 mg/1	500 TABLET in 1 BOTTLE (16571-775-50)
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)
65862-579-01	65862-579	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20120629	N/A	ANDA	ANDA202759	Aurobindo Pharma Limited	GLIMEPIRIDE	1 mg/1	100 TABLET in 1 BOTTLE (65862-579-01)
65862-579-05	65862-579	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20120629	N/A	ANDA	ANDA202759	Aurobindo Pharma Limited	GLIMEPIRIDE	1 mg/1	500 TABLET in 1 BOTTLE (65862-579-05)
65862-579-99	65862-579	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20120629	N/A	ANDA	ANDA202759	Aurobindo Pharma Limited	GLIMEPIRIDE	1 mg/1	1000 TABLET in 1 BOTTLE (65862-579-99)
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)