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
0093-1024-06	0093-1024	HUMAN PRESCRIPTION DRUG	Nefazodone Hydrochloride	Nefazodone Hydrochloride	TABLET	ORAL	20030916	N/A	ANDA	ANDA076037	Teva Pharmaceuticals USA, Inc.	NEFAZODONE HYDROCHLORIDE	100 mg/1	60 TABLET in 1 BOTTLE (0093-1024-06)
0093-1025-06	0093-1025	HUMAN PRESCRIPTION DRUG	Nefazodone Hydrochloride	Nefazodone Hydrochloride	TABLET	ORAL	20030916	N/A	ANDA	ANDA076037	Teva Pharmaceuticals USA, Inc.	NEFAZODONE HYDROCHLORIDE	200 mg/1	60 TABLET in 1 BOTTLE (0093-1025-06)
0093-1026-06	0093-1026	HUMAN PRESCRIPTION DRUG	Nefazodone Hydrochloride	Nefazodone Hydrochloride	TABLET	ORAL	20030916	N/A	ANDA	ANDA076037	Teva Pharmaceuticals USA, Inc.	NEFAZODONE HYDROCHLORIDE	250 mg/1	60 TABLET in 1 BOTTLE (0093-1026-06)
0093-7113-06	0093-7113	HUMAN PRESCRIPTION DRUG	Nefazodone Hydrochloride	Nefazodone Hydrochloride	TABLET	ORAL	20030916	N/A	ANDA	ANDA076037	Teva Pharmaceuticals USA, Inc.	NEFAZODONE HYDROCHLORIDE	150 mg/1	60 TABLET in 1 BOTTLE (0093-7113-06)
0093-7178-01	0093-7178	HUMAN PRESCRIPTION DRUG	Nefazodone Hydrochloride	Nefazodone Hydrochloride	TABLET	ORAL	20030916	N/A	ANDA	ANDA076037	Teva Pharmaceuticals USA, Inc.	NEFAZODONE HYDROCHLORIDE	50 mg/1	100 TABLET in 1 BOTTLE (0093-7178-01)