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
71335-9629-0	71335-9629	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	Zolpidem Tartrate	TABLET, COATED	ORAL	20230123	N/A	ANDA	ANDA077322	Bryant Ranch Prepack	ZOLPIDEM TARTRATE	5 mg/1	25 TABLET, COATED in 1 BOTTLE (71335-9629-0)
0781-5317-01	0781-5317	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	Zolpidem Tartrate	TABLET, COATED	ORAL	20070423	N/A	ANDA	ANDA077322	Sandoz Inc	ZOLPIDEM TARTRATE	5 mg/1	100 TABLET, COATED in 1 BOTTLE (0781-5317-01)
0781-5318-01	0781-5318	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	Zolpidem Tartrate	TABLET, COATED	ORAL	20070423	N/A	ANDA	ANDA077322	Sandoz Inc	ZOLPIDEM TARTRATE	10 mg/1	100 TABLET, COATED in 1 BOTTLE (0781-5318-01)
0781-5318-05	0781-5318	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	Zolpidem Tartrate	TABLET, COATED	ORAL	20070423	N/A	ANDA	ANDA077322	Sandoz Inc	ZOLPIDEM TARTRATE	10 mg/1	500 TABLET, COATED in 1 BOTTLE (0781-5318-05)
0781-5318-10	0781-5318	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	Zolpidem Tartrate	TABLET, COATED	ORAL	20070423	N/A	ANDA	ANDA077322	Sandoz Inc	ZOLPIDEM TARTRATE	10 mg/1	1000 TABLET, COATED in 1 BOTTLE (0781-5318-10)
0781-5318-31	0781-5318	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	Zolpidem Tartrate	TABLET, COATED	ORAL	20070423	N/A	ANDA	ANDA077322	Sandoz Inc	ZOLPIDEM TARTRATE	10 mg/1	30 TABLET, COATED in 1 BOTTLE (0781-5318-31)
80425-0513-1	80425-0513	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	Zolpidem Tartrate	TABLET, COATED	ORAL	20250415	N/A	ANDA	ANDA077322	Advanced Rx of Tennessee, LLC	ZOLPIDEM TARTRATE	5 mg/1	30 TABLET, COATED in 1 BOTTLE (80425-0513-1)
80425-0513-2	80425-0513	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	Zolpidem Tartrate	TABLET, COATED	ORAL	20250415	N/A	ANDA	ANDA077322	Advanced Rx of Tennessee, LLC	ZOLPIDEM TARTRATE	5 mg/1	60 TABLET, COATED in 1 BOTTLE (80425-0513-2)
80425-0513-3	80425-0513	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	Zolpidem Tartrate	TABLET, COATED	ORAL	20250415	N/A	ANDA	ANDA077322	Advanced Rx of Tennessee, LLC	ZOLPIDEM TARTRATE	5 mg/1	90 TABLET, COATED in 1 BOTTLE (80425-0513-3)
0781-5317-05	0781-5317	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	Zolpidem Tartrate	TABLET, COATED	ORAL	20070423	N/A	ANDA	ANDA077322	Sandoz Inc	ZOLPIDEM TARTRATE	5 mg/1	500 TABLET, COATED in 1 BOTTLE (0781-5317-05)
0781-5317-10	0781-5317	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	Zolpidem Tartrate	TABLET, COATED	ORAL	20070423	N/A	ANDA	ANDA077322	Sandoz Inc	ZOLPIDEM TARTRATE	5 mg/1	1000 TABLET, COATED in 1 BOTTLE (0781-5317-10)
0781-5317-31	0781-5317	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	Zolpidem Tartrate	TABLET, COATED	ORAL	20070423	N/A	ANDA	ANDA077322	Sandoz Inc	ZOLPIDEM TARTRATE	5 mg/1	30 TABLET, COATED in 1 BOTTLE (0781-5317-31)
82868-078-30	82868-078	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	Zolpidem Tartrate	TABLET, COATED	ORAL	20250520	N/A	ANDA	ANDA077322	Northwind Health Company, LLC	ZOLPIDEM TARTRATE	10 mg/1	30 TABLET, COATED in 1 BOTTLE, PLASTIC (82868-078-30)
70518-3739-0	70518-3739	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	Zolpidem Tartrate	TABLET, COATED	ORAL	20230531	N/A	ANDA	ANDA077322	REMEDYREPACK INC.	ZOLPIDEM TARTRATE	10 mg/1	30 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3739-0)
60760-761-30	60760-761	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	Zolpidem Tartrate	TABLET, COATED	ORAL	20250807	N/A	ANDA	ANDA077322	ST. MARY'S MEDICAL PARK PHARMACY	ZOLPIDEM TARTRATE	5 mg/1	30 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-761-30)