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
71921-214-50	71921-214	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20230731	N/A	ANDA	ANDA202112	Florida Pharmaceutical Products, LLC	GLIMEPIRIDE	1 mg/1	500 TABLET in 1 BOTTLE (71921-214-50)
71921-215-01	71921-215	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20230731	N/A	ANDA	ANDA202112	Florida Pharmaceutical Products, LLC	GLIMEPIRIDE	2 mg/1	100 TABLET in 1 BOTTLE (71921-215-01)
71921-215-50	71921-215	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20230731	N/A	ANDA	ANDA202112	Florida Pharmaceutical Products, LLC	GLIMEPIRIDE	2 mg/1	500 TABLET in 1 BOTTLE (71921-215-50)
71921-216-01	71921-216	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20230731	N/A	ANDA	ANDA202112	Florida Pharmaceutical Products, LLC	GLIMEPIRIDE	4 mg/1	100 TABLET in 1 BOTTLE (71921-216-01)
71921-216-50	71921-216	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20230731	N/A	ANDA	ANDA202112	Florida Pharmaceutical Products, LLC	GLIMEPIRIDE	4 mg/1	500 TABLET in 1 BOTTLE (71921-216-50)
67046-1608-3	67046-1608	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20251022	N/A	ANDA	ANDA202112	Coupler LLC	GLIMEPIRIDE	2 mg/1	30 TABLET in 1 BLISTER PACK (67046-1608-3)
72189-585-90	72189-585	HUMAN PRESCRIPTION DRUG	Glimepiride	Glimepiride	TABLET	ORAL	20240926	N/A	ANDA	ANDA202112	Direct_rx	GLIMEPIRIDE	4 mg/1	90 TABLET in 1 BOTTLE (72189-585-90)