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
33342-299-44	33342-299	HUMAN PRESCRIPTION DRUG	Eszopiclone	Eszopiclone	TABLET, FILM COATED	ORAL	20150131	N/A	ANDA	ANDA202929	Macleods Pharmaceuticals Limited	ESZOPICLONE	1 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (33342-299-44)
63187-843-30	63187-843	HUMAN PRESCRIPTION DRUG	Eszopiclone	Eszopiclone	TABLET, FILM COATED	ORAL	20170501	N/A	ANDA	ANDA202929	Proficient Rx LP	ESZOPICLONE	3 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-843-30)
63187-843-60	63187-843	HUMAN PRESCRIPTION DRUG	Eszopiclone	Eszopiclone	TABLET, FILM COATED	ORAL	20170501	N/A	ANDA	ANDA202929	Proficient Rx LP	ESZOPICLONE	3 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63187-843-60)
63187-843-90	63187-843	HUMAN PRESCRIPTION DRUG	Eszopiclone	Eszopiclone	TABLET, FILM COATED	ORAL	20170501	N/A	ANDA	ANDA202929	Proficient Rx LP	ESZOPICLONE	3 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63187-843-90)
68788-7029-2	68788-7029	HUMAN PRESCRIPTION DRUG	Eszopiclone	Eszopiclone	TABLET, FILM COATED	ORAL	20171012	N/A	ANDA	ANDA202929	Preferred Pharmaceuticals Inc.	ESZOPICLONE	2 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (68788-7029-2)
68788-7029-3	68788-7029	HUMAN PRESCRIPTION DRUG	Eszopiclone	Eszopiclone	TABLET, FILM COATED	ORAL	20171012	N/A	ANDA	ANDA202929	Preferred Pharmaceuticals Inc.	ESZOPICLONE	2 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-7029-3)
68788-7029-6	68788-7029	HUMAN PRESCRIPTION DRUG	Eszopiclone	Eszopiclone	TABLET, FILM COATED	ORAL	20171012	N/A	ANDA	ANDA202929	Preferred Pharmaceuticals Inc.	ESZOPICLONE	2 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-7029-6)
68788-7029-9	68788-7029	HUMAN PRESCRIPTION DRUG	Eszopiclone	Eszopiclone	TABLET, FILM COATED	ORAL	20171012	N/A	ANDA	ANDA202929	Preferred Pharmaceuticals Inc.	ESZOPICLONE	2 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-7029-9)