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
63629-2948-7	63629-2948	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20211222	N/A	ANDA	ANDA071307	Bryant Ranch Prepack	DIAZEPAM	2 mg/1	2 TABLET in 1 BOTTLE (63629-2948-7)
63629-2948-8	63629-2948	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20171101	N/A	ANDA	ANDA071307	Bryant Ranch Prepack	DIAZEPAM	2 mg/1	15 TABLET in 1 BOTTLE (63629-2948-8)
63629-2948-9	63629-2948	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20171101	N/A	ANDA	ANDA071307	Bryant Ranch Prepack	DIAZEPAM	2 mg/1	45 TABLET in 1 BOTTLE (63629-2948-9)
0172-3925-60	0172-3925	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	19861210	N/A	ANDA	ANDA071307	Teva Pharmaceuticals USA, Inc.	DIAZEPAM	2 mg/1	100 TABLET in 1 BOTTLE (0172-3925-60)
0172-3925-70	0172-3925	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20001018	N/A	ANDA	ANDA071307	Teva Pharmaceuticals USA, Inc.	DIAZEPAM	2 mg/1	500 TABLET in 1 BOTTLE (0172-3925-70)
50090-0195-6	50090-0195	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20141128	N/A	ANDA	ANDA071307	A-S Medication Solutions	DIAZEPAM	2 mg/1	2 TABLET in 1 BOTTLE (50090-0195-6)
58118-3925-8	58118-3925	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20190809	N/A	ANDA	ANDA071307	Clinical Solutions Wholesale, LLC	DIAZEPAM	2 mg/1	30 TABLET in 1 BLISTER PACK (58118-3925-8)
43063-840-30	43063-840	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20180322	N/A	ANDA	ANDA071307	PD-Rx Pharmaceuticals, Inc.	DIAZEPAM	2 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (43063-840-30)