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
63187-377-30	63187-377	HUMAN PRESCRIPTION DRUG	Trazodone Hydrochloride	Trazodone Hydrochloride	TABLET, FILM COATED	ORAL	20160901	N/A	ANDA	ANDA072193	Proficient Rx LP	TRAZODONE HYDROCHLORIDE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63187-377-30)
63187-377-60	63187-377	HUMAN PRESCRIPTION DRUG	Trazodone Hydrochloride	Trazodone Hydrochloride	TABLET, FILM COATED	ORAL	20160901	N/A	ANDA	ANDA072193	Proficient Rx LP	TRAZODONE HYDROCHLORIDE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63187-377-60)
63187-377-90	63187-377	HUMAN PRESCRIPTION DRUG	Trazodone Hydrochloride	Trazodone Hydrochloride	TABLET, FILM COATED	ORAL	20160901	N/A	ANDA	ANDA072193	Proficient Rx LP	TRAZODONE HYDROCHLORIDE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63187-377-90)
69584-885-90	69584-885	HUMAN PRESCRIPTION DRUG	Trazodone Hydrochloride	Trazodone Hydrochloride	TABLET, FILM COATED	ORAL	20230301	N/A	ANDA	ANDA072193	Oxford Pharmaceuticals, LLC	TRAZODONE HYDROCHLORIDE	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69584-885-90)
69584-885-50	69584-885	HUMAN PRESCRIPTION DRUG	Trazodone Hydrochloride	Trazodone Hydrochloride	TABLET, FILM COATED	ORAL	20230301	N/A	ANDA	ANDA072193	Oxford Pharmaceuticals, LLC	TRAZODONE HYDROCHLORIDE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69584-885-50)
69584-885-10	69584-885	HUMAN PRESCRIPTION DRUG	Trazodone Hydrochloride	Trazodone Hydrochloride	TABLET, FILM COATED	ORAL	20230301	N/A	ANDA	ANDA072193	Oxford Pharmaceuticals, LLC	TRAZODONE HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69584-885-10)