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
68180-324-01	68180-324	HUMAN PRESCRIPTION DRUG	Eszopiclone	Eszopiclone	TABLET, FILM COATED	ORAL	20140415	N/A	ANDA	ANDA091124	Lupin Pharmaceuticals, Inc.	ESZOPICLONE	3 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68180-324-01)
68180-323-01	68180-323	HUMAN PRESCRIPTION DRUG	Eszopiclone	Eszopiclone	TABLET, FILM COATED	ORAL	20140415	N/A	ANDA	ANDA091124	Lupin Pharmaceuticals, Inc.	ESZOPICLONE	2 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68180-323-01)
68180-322-01	68180-322	HUMAN PRESCRIPTION DRUG	Eszopiclone	Eszopiclone	TABLET, FILM COATED	ORAL	20140415	N/A	ANDA	ANDA091124	Lupin Pharmaceuticals, Inc.	ESZOPICLONE	1 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68180-322-01)
43063-795-30	43063-795	HUMAN PRESCRIPTION DRUG	Eszopiclone	Eszopiclone	TABLET, FILM COATED	ORAL	20171009	N/A	ANDA	ANDA091124	PD-Rx Pharmaceuticals, Inc.	ESZOPICLONE	3 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-795-30)
72189-099-30	72189-099	HUMAN PRESCRIPTION DRUG	ESZOPICLONE	ESZOPICLONE	TABLET, FILM COATED	ORAL	20200610	N/A	ANDA	ANDA091124	DIRECT RX	ESZOPICLONE	1 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72189-099-30)
72189-099-90	72189-099	HUMAN PRESCRIPTION DRUG	ESZOPICLONE	ESZOPICLONE	TABLET, FILM COATED	ORAL	20200610	N/A	ANDA	ANDA091124	DIRECT RX	ESZOPICLONE	1 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72189-099-90)
80425-0115-1	80425-0115	HUMAN PRESCRIPTION DRUG	Eszopiclone	Eszopiclone	TABLET, FILM COATED	ORAL	20140415	N/A	ANDA	ANDA091124	Advanced Rx Pharmacy of Tennessee, LLC	ESZOPICLONE	3 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0115-1)
80425-0098-1	80425-0098	HUMAN PRESCRIPTION DRUG	Eszopiclone	Eszopiclone	TABLET, FILM COATED	ORAL	20140415	N/A	ANDA	ANDA091124	Advanced Rx Pharmacy of Tennessee, LLC	ESZOPICLONE	1 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0098-1)