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
72603-222-01	72603-222	HUMAN PRESCRIPTION DRUG	Doxepin	Doxepin	TABLET, FILM COATED	ORAL	20240401	N/A	ANDA	ANDA202337	North Star Rx LLC	DOXEPIN HYDROCHLORIDE	3 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72603-222-01)
72603-223-01	72603-223	HUMAN PRESCRIPTION DRUG	Doxepin	Doxepin	TABLET, FILM COATED	ORAL	20240401	N/A	ANDA	ANDA202337	North Star Rx LLC	DOXEPIN HYDROCHLORIDE	6 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72603-223-01)
10135-758-30	10135-758	HUMAN PRESCRIPTION DRUG	Doxepin	Doxepin	TABLET, FILM COATED	ORAL	20231001	N/A	ANDA	ANDA202337	Marlex Pharmaceuticals, Inc.	DOXEPIN HYDROCHLORIDE	3 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (10135-758-30)
10135-764-30	10135-764	HUMAN PRESCRIPTION DRUG	Doxepin	Doxepin	TABLET, FILM COATED	ORAL	20231001	N/A	ANDA	ANDA202337	Marlex Pharmaceuticals, Inc.	DOXEPIN HYDROCHLORIDE	6 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (10135-764-30)
72819-161-03	72819-161	HUMAN PRESCRIPTION DRUG	Doxepin	Doxepin	TABLET, FILM COATED	ORAL	20220221	N/A	ANDA	ANDA202337	Archis Pharma LLC	DOXEPIN HYDROCHLORIDE	3 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72819-161-03)
72819-161-10	72819-161	HUMAN PRESCRIPTION DRUG	Doxepin	Doxepin	TABLET, FILM COATED	ORAL	20220221	N/A	ANDA	ANDA202337	Archis Pharma LLC	DOXEPIN HYDROCHLORIDE	3 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72819-161-10)
72819-161-11	72819-161	HUMAN PRESCRIPTION DRUG	Doxepin	Doxepin	TABLET, FILM COATED	ORAL	20220221	N/A	ANDA	ANDA202337	Archis Pharma LLC	DOXEPIN HYDROCHLORIDE	3 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72819-161-11)
72819-162-03	72819-162	HUMAN PRESCRIPTION DRUG	Doxepin	Doxepin	TABLET, FILM COATED	ORAL	20220221	N/A	ANDA	ANDA202337	Archis Pharma LLC	DOXEPIN HYDROCHLORIDE	6 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72819-162-03)
72819-162-10	72819-162	HUMAN PRESCRIPTION DRUG	Doxepin	Doxepin	TABLET, FILM COATED	ORAL	20220221	N/A	ANDA	ANDA202337	Archis Pharma LLC	DOXEPIN HYDROCHLORIDE	6 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72819-162-10)
72819-162-11	72819-162	HUMAN PRESCRIPTION DRUG	Doxepin	Doxepin	TABLET, FILM COATED	ORAL	20220221	N/A	ANDA	ANDA202337	Archis Pharma LLC	DOXEPIN HYDROCHLORIDE	6 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72819-162-11)