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
0955-1702-10	0955-1702	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	zolpidem tartrate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20101014	20260430	NDA AUTHORIZED GENERIC	NDA021774	Sanofi-Aventis U.S. LLC	ZOLPIDEM TARTRATE	6.25 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0955-1702-10)
51407-761-01	51407-761	HUMAN PRESCRIPTION DRUG	zolpidem tartrate	zolpidem tartrate	TABLET, COATED	ORAL	20250826	N/A	NDA	NDA021774	Golden State Medical Supply, Inc.	ZOLPIDEM TARTRATE	6.25 mg/1	100 TABLET, COATED in 1 BOTTLE (51407-761-01)
51407-762-01	51407-762	HUMAN PRESCRIPTION DRUG	zolpidem tartrate	zolpidem tartrate	TABLET, COATED	ORAL	20250826	N/A	NDA	NDA021774	Golden State Medical Supply, Inc.	ZOLPIDEM TARTRATE	12.5 mg/1	100 TABLET, COATED in 1 BOTTLE (51407-762-01)
0713-5501-01	0713-5501	HUMAN PRESCRIPTION DRUG	Ambien CR	zolpidem tartrate	TABLET, COATED	ORAL	20250207	N/A	NDA	NDA021774	Cosette Pharmaceuticals, Inc.	ZOLPIDEM TARTRATE	6.25 mg/1	100 TABLET, COATED in 1 BOTTLE (0713-5501-01)
71610-770-15	71610-770	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	zolpidem tartrate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240119	N/A	NDA AUTHORIZED GENERIC	NDA021774	Aphena Pharma Solutions - Tennessee, LLC	ZOLPIDEM TARTRATE	6.25 mg/1	15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-770-15)
71610-770-28	71610-770	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	zolpidem tartrate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240119	N/A	NDA AUTHORIZED GENERIC	NDA021774	Aphena Pharma Solutions - Tennessee, LLC	ZOLPIDEM TARTRATE	6.25 mg/1	28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-770-28)
71610-770-30	71610-770	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	zolpidem tartrate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240119	N/A	NDA AUTHORIZED GENERIC	NDA021774	Aphena Pharma Solutions - Tennessee, LLC	ZOLPIDEM TARTRATE	6.25 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-770-30)
71610-770-53	71610-770	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	zolpidem tartrate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240119	N/A	NDA AUTHORIZED GENERIC	NDA021774	Aphena Pharma Solutions - Tennessee, LLC	ZOLPIDEM TARTRATE	6.25 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-770-53)
71610-770-60	71610-770	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	zolpidem tartrate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240119	N/A	NDA AUTHORIZED GENERIC	NDA021774	Aphena Pharma Solutions - Tennessee, LLC	ZOLPIDEM TARTRATE	6.25 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-770-60)
0024-5501-31	0024-5501	HUMAN PRESCRIPTION DRUG	Ambien CR	zolpidem tartrate	TABLET, COATED	ORAL	20050919	20260430	NDA	NDA021774	Sanofi-Aventis U.S. LLC	ZOLPIDEM TARTRATE	6.25 mg/1	100 TABLET, COATED in 1 BOTTLE (0024-5501-31)
0713-5521-01	0713-5521	HUMAN PRESCRIPTION DRUG	Ambien CR	zolpidem tartrate	TABLET, COATED	ORAL	20250207	N/A	NDA	NDA021774	Cosette Pharmaceuticals, Inc.	ZOLPIDEM TARTRATE	12.5 mg/1	100 TABLET, COATED in 1 BOTTLE (0713-5521-01)
0955-1703-10	0955-1703	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	zolpidem tartrate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20101206	20260531	NDA AUTHORIZED GENERIC	NDA021774	Sanofi-Aventis U.S. LLC	ZOLPIDEM TARTRATE	12.5 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0955-1703-10)
63187-862-15	63187-862	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	zolpidem tartrate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170601	N/A	NDA AUTHORIZED GENERIC	NDA021774	Proficient Rx LP	ZOLPIDEM TARTRATE	12.5 mg/1	15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-862-15)
63187-862-30	63187-862	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	zolpidem tartrate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170601	N/A	NDA AUTHORIZED GENERIC	NDA021774	Proficient Rx LP	ZOLPIDEM TARTRATE	12.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-862-30)
63187-862-60	63187-862	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	zolpidem tartrate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170601	N/A	NDA AUTHORIZED GENERIC	NDA021774	Proficient Rx LP	ZOLPIDEM TARTRATE	12.5 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-862-60)
63187-862-90	63187-862	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	zolpidem tartrate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170601	N/A	NDA AUTHORIZED GENERIC	NDA021774	Proficient Rx LP	ZOLPIDEM TARTRATE	12.5 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-862-90)
0024-5521-31	0024-5521	HUMAN PRESCRIPTION DRUG	Ambien CR	zolpidem tartrate	TABLET, COATED	ORAL	20050919	20260731	NDA	NDA021774	Sanofi-Aventis U.S. LLC	ZOLPIDEM TARTRATE	12.5 mg/1	100 TABLET, COATED in 1 BOTTLE (0024-5521-31)
43353-727-30	43353-727	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	zolpidem tartrate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20110514	N/A	NDA AUTHORIZED GENERIC	NDA021774	Aphena Pharma Solutions - Tennessee, LLC	ZOLPIDEM TARTRATE	12.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43353-727-30)
43353-727-60	43353-727	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	zolpidem tartrate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20111016	N/A	NDA AUTHORIZED GENERIC	NDA021774	Aphena Pharma Solutions - Tennessee, LLC	ZOLPIDEM TARTRATE	12.5 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43353-727-60)