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
0093-0812-01	0093-0812	HUMAN PRESCRIPTION DRUG	Nortriptyline Hydrochloride	Nortriptyline Hydrochloride	CAPSULE	ORAL	19950405	N/A	ANDA	ANDA074132	Teva Pharmaceuticals USA, Inc.	NORTRIPTYLINE HYDROCHLORIDE	50 mg/1	100 CAPSULE in 1 BOTTLE (0093-0812-01)
0093-0812-05	0093-0812	HUMAN PRESCRIPTION DRUG	Nortriptyline Hydrochloride	Nortriptyline Hydrochloride	CAPSULE	ORAL	19950406	N/A	ANDA	ANDA074132	Teva Pharmaceuticals USA, Inc.	NORTRIPTYLINE HYDROCHLORIDE	50 mg/1	500 CAPSULE in 1 BOTTLE (0093-0812-05)
0093-0813-01	0093-0813	HUMAN PRESCRIPTION DRUG	Nortriptyline Hydrochloride	Nortriptyline Hydrochloride	CAPSULE	ORAL	19950405	N/A	ANDA	ANDA074132	Teva Pharmaceuticals USA, Inc.	NORTRIPTYLINE HYDROCHLORIDE	75 mg/1	100 CAPSULE in 1 BOTTLE (0093-0813-01)
0093-0813-05	0093-0813	HUMAN PRESCRIPTION DRUG	Nortriptyline Hydrochloride	Nortriptyline Hydrochloride	CAPSULE	ORAL	19950406	20260430	ANDA	ANDA074132	Teva Pharmaceuticals USA, Inc.	NORTRIPTYLINE HYDROCHLORIDE	75 mg/1	500 CAPSULE in 1 BOTTLE (0093-0813-05)