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
80425-0386-1	80425-0386	HUMAN PRESCRIPTION DRUG	Amitriptyline Hydrochloride	Amitriptyline Hydrochloride	TABLET, FILM COATED	ORAL	20240521	N/A	ANDA	ANDA214548	Advanced Rx of Tennessee, LLC	AMITRIPTYLINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0386-1)
80425-0386-2	80425-0386	HUMAN PRESCRIPTION DRUG	Amitriptyline Hydrochloride	Amitriptyline Hydrochloride	TABLET, FILM COATED	ORAL	20240521	N/A	ANDA	ANDA214548	Advanced Rx of Tennessee, LLC	AMITRIPTYLINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0386-2)
80425-0386-3	80425-0386	HUMAN PRESCRIPTION DRUG	Amitriptyline Hydrochloride	Amitriptyline Hydrochloride	TABLET, FILM COATED	ORAL	20240521	N/A	ANDA	ANDA214548	Advanced Rx of Tennessee, LLC	AMITRIPTYLINE HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (80425-0386-3)
76420-696-30	76420-696	HUMAN PRESCRIPTION DRUG	Amitriptyline Hydrochloride	Amitriptyline Hydrochloride	TABLET, FILM COATED	ORAL	20240302	N/A	ANDA	ANDA214548	Asclemed USA, Inc.	AMITRIPTYLINE HYDROCHLORIDE	75 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-696-30)
76420-696-60	76420-696	HUMAN PRESCRIPTION DRUG	Amitriptyline Hydrochloride	Amitriptyline Hydrochloride	TABLET, FILM COATED	ORAL	20240302	N/A	ANDA	ANDA214548	Asclemed USA, Inc.	AMITRIPTYLINE HYDROCHLORIDE	75 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (76420-696-60)
76420-696-90	76420-696	HUMAN PRESCRIPTION DRUG	Amitriptyline Hydrochloride	Amitriptyline Hydrochloride	TABLET, FILM COATED	ORAL	20240302	N/A	ANDA	ANDA214548	Asclemed USA, Inc.	AMITRIPTYLINE HYDROCHLORIDE	75 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (76420-696-90)