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
0172-3926-80	0172-3926	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	19861210	N/A	ANDA	ANDA071321	Teva Pharmaceuticals USA, Inc.	DIAZEPAM	5 mg/1	1000 TABLET in 1 BOTTLE (0172-3926-80)
68071-4922-1	68071-4922	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20190613	N/A	ANDA	ANDA071321	NuCare Pharmaceuticals,Inc.	DIAZEPAM	5 mg/1	10 TABLET in 1 BOTTLE (68071-4922-1)
68071-4922-4	68071-4922	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20190613	N/A	ANDA	ANDA071321	NuCare Pharmaceuticals,Inc.	DIAZEPAM	5 mg/1	8 TABLET in 1 BOTTLE (68071-4922-4)
68071-4922-6	68071-4922	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20190613	N/A	ANDA	ANDA071321	NuCare Pharmaceuticals,Inc.	DIAZEPAM	5 mg/1	6 TABLET in 1 BOTTLE (68071-4922-6)