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
57664-745-13	57664-745	HUMAN PRESCRIPTION DRUG	Repaglinide	Repaglinide	TABLET	ORAL	20130711	N/A	ANDA	ANDA077571	Sun Pharmaceutical Industries, Inc.	REPAGLINIDE	1 mg/1	500 TABLET in 1 BOTTLE (57664-745-13)
57664-745-18	57664-745	HUMAN PRESCRIPTION DRUG	Repaglinide	Repaglinide	TABLET	ORAL	20130711	N/A	ANDA	ANDA077571	Sun Pharmaceutical Industries, Inc.	REPAGLINIDE	1 mg/1	1000 TABLET in 1 BOTTLE (57664-745-18)
57664-745-88	57664-745	HUMAN PRESCRIPTION DRUG	Repaglinide	Repaglinide	TABLET	ORAL	20130711	N/A	ANDA	ANDA077571	Sun Pharmaceutical Industries, Inc.	REPAGLINIDE	1 mg/1	100 TABLET in 1 BOTTLE (57664-745-88)
57664-747-13	57664-747	HUMAN PRESCRIPTION DRUG	Repaglinide	Repaglinide	TABLET	ORAL	20130711	N/A	ANDA	ANDA077571	Sun Pharmaceutical Industries, Inc.	REPAGLINIDE	2 mg/1	500 TABLET in 1 BOTTLE (57664-747-13)
57664-747-18	57664-747	HUMAN PRESCRIPTION DRUG	Repaglinide	Repaglinide	TABLET	ORAL	20130711	N/A	ANDA	ANDA077571	Sun Pharmaceutical Industries, Inc.	REPAGLINIDE	2 mg/1	1000 TABLET in 1 BOTTLE (57664-747-18)
57664-747-88	57664-747	HUMAN PRESCRIPTION DRUG	Repaglinide	Repaglinide	TABLET	ORAL	20130711	N/A	ANDA	ANDA077571	Sun Pharmaceutical Industries, Inc.	REPAGLINIDE	2 mg/1	100 TABLET in 1 BOTTLE (57664-747-88)