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
0024-5421-31	0024-5421	HUMAN PRESCRIPTION DRUG	Ambien	zolpidem tartrate	TABLET, FILM COATED	ORAL	19930401	20260930	NDA	NDA019908	Sanofi-Aventis U.S. LLC	ZOLPIDEM TARTRATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0024-5421-31)
0024-5401-31	0024-5401	HUMAN PRESCRIPTION DRUG	Ambien	zolpidem tartrate	TABLET, FILM COATED	ORAL	19930401	20261031	NDA	NDA019908	Sanofi-Aventis U.S. LLC	ZOLPIDEM TARTRATE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0024-5401-31)
0713-5421-01	0713-5421	HUMAN PRESCRIPTION DRUG	Ambien	zolpidem tartrate	TABLET, FILM COATED	ORAL	20250207	N/A	NDA	NDA019908	Cosette Pharmaceuticals, Inc.	ZOLPIDEM TARTRATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0713-5421-01)
0713-5401-01	0713-5401	HUMAN PRESCRIPTION DRUG	Ambien	zolpidem tartrate	TABLET, FILM COATED	ORAL	20250207	N/A	NDA	NDA019908	Cosette Pharmaceuticals, Inc.	ZOLPIDEM TARTRATE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0713-5401-01)