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
70710-1156-5	70710-1156	HUMAN PRESCRIPTION DRUG	Nortriptyline Hydrochloride	Nortriptyline Hydrochloride	CAPSULE	ORAL	20220210	N/A	ANDA	ANDA213441	Zydus Pharmaceuticals (USA) Inc.	NORTRIPTYLINE HYDROCHLORIDE	75 mg/1	500 CAPSULE in 1 BOTTLE (70710-1156-5)
70771-1615-1	70771-1615	HUMAN PRESCRIPTION DRUG	Nortriptyline Hydrochloride	Nortriptyline Hydrochloride	CAPSULE	ORAL	20220210	N/A	ANDA	ANDA213441	Zydus Lifesciences Limited	NORTRIPTYLINE HYDROCHLORIDE	75 mg/1	100 CAPSULE in 1 BOTTLE (70771-1615-1)
70771-1615-3	70771-1615	HUMAN PRESCRIPTION DRUG	Nortriptyline Hydrochloride	Nortriptyline Hydrochloride	CAPSULE	ORAL	20220210	N/A	ANDA	ANDA213441	Zydus Lifesciences Limited	NORTRIPTYLINE HYDROCHLORIDE	75 mg/1	30 CAPSULE in 1 BOTTLE (70771-1615-3)
70771-1615-5	70771-1615	HUMAN PRESCRIPTION DRUG	Nortriptyline Hydrochloride	Nortriptyline Hydrochloride	CAPSULE	ORAL	20220210	N/A	ANDA	ANDA213441	Zydus Lifesciences Limited	NORTRIPTYLINE HYDROCHLORIDE	75 mg/1	500 CAPSULE in 1 BOTTLE (70771-1615-5)