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
42806-097-01	42806-097	HUMAN PRESCRIPTION DRUG	Protriptyline Hydrochloride	Protriptyline Hydrochloride	TABLET, FILM COATED	ORAL	20130109	N/A	ANDA	ANDA202220	Epic Pharma, LLC	PROTRIPTYLINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (42806-097-01)
42806-097-10	42806-097	HUMAN PRESCRIPTION DRUG	Protriptyline Hydrochloride	Protriptyline Hydrochloride	TABLET, FILM COATED	ORAL	20130109	N/A	ANDA	ANDA202220	Epic Pharma, LLC	PROTRIPTYLINE HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (42806-097-10)
42806-097-30	42806-097	HUMAN PRESCRIPTION DRUG	Protriptyline Hydrochloride	Protriptyline Hydrochloride	TABLET, FILM COATED	ORAL	20200710	N/A	ANDA	ANDA202220	Epic Pharma, LLC	PROTRIPTYLINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (42806-097-30)
42806-096-01	42806-096	HUMAN PRESCRIPTION DRUG	Protriptyline Hydrochloride	Protriptyline Hydrochloride	TABLET, FILM COATED	ORAL	20130109	N/A	ANDA	ANDA202220	Epic Pharma, LLC	PROTRIPTYLINE HYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (42806-096-01)
42806-096-10	42806-096	HUMAN PRESCRIPTION DRUG	Protriptyline Hydrochloride	Protriptyline Hydrochloride	TABLET, FILM COATED	ORAL	20130109	N/A	ANDA	ANDA202220	Epic Pharma, LLC	PROTRIPTYLINE HYDROCHLORIDE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (42806-096-10)
42806-096-30	42806-096	HUMAN PRESCRIPTION DRUG	Protriptyline Hydrochloride	Protriptyline Hydrochloride	TABLET, FILM COATED	ORAL	20200710	N/A	ANDA	ANDA202220	Epic Pharma, LLC	PROTRIPTYLINE HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (42806-096-30)