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
57664-014-72	57664-014	HUMAN PRESCRIPTION DRUG	Trazodone Hydrochloride	Trazodone Hydrochloride	TABLET, FILM COATED	ORAL	20221003	N/A	ANDA	ANDA073137	Sun Pharmaceutical Industries, Inc.	TRAZODONE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-014-72)
57664-014-74	57664-014	HUMAN PRESCRIPTION DRUG	Trazodone Hydrochloride	Trazodone Hydrochloride	TABLET, FILM COATED	ORAL	20221003	N/A	ANDA	ANDA073137	Sun Pharmaceutical Industries, Inc.	TRAZODONE HYDROCHLORIDE	50 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-014-74)
57664-014-75	57664-014	HUMAN PRESCRIPTION DRUG	Trazodone Hydrochloride	Trazodone Hydrochloride	TABLET, FILM COATED	ORAL	20221003	N/A	ANDA	ANDA073137	Sun Pharmaceutical Industries, Inc.	TRAZODONE HYDROCHLORIDE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-014-75)
57664-026-72	57664-026	HUMAN PRESCRIPTION DRUG	Trazodone Hydrochloride	Trazodone Hydrochloride	TABLET, FILM COATED	ORAL	20221003	N/A	ANDA	ANDA073137	Sun Pharmaceutical Industries, Inc.	TRAZODONE HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-026-72)
57664-026-74	57664-026	HUMAN PRESCRIPTION DRUG	Trazodone Hydrochloride	Trazodone Hydrochloride	TABLET, FILM COATED	ORAL	20221003	N/A	ANDA	ANDA073137	Sun Pharmaceutical Industries, Inc.	TRAZODONE HYDROCHLORIDE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-026-74)
57664-026-75	57664-026	HUMAN PRESCRIPTION DRUG	Trazodone Hydrochloride	Trazodone Hydrochloride	TABLET, FILM COATED	ORAL	20221003	N/A	ANDA	ANDA073137	Sun Pharmaceutical Industries, Inc.	TRAZODONE HYDROCHLORIDE	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-026-75)
57664-053-72	57664-053	HUMAN PRESCRIPTION DRUG	Trazodone Hydrochloride	Trazodone Hydrochloride	TABLET	ORAL	20221003	N/A	ANDA	ANDA073137	Sun Pharmaceutical Industries, Inc.	TRAZODONE HYDROCHLORIDE	150 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (57664-053-72)
57664-053-74	57664-053	HUMAN PRESCRIPTION DRUG	Trazodone Hydrochloride	Trazodone Hydrochloride	TABLET	ORAL	20221003	N/A	ANDA	ANDA073137	Sun Pharmaceutical Industries, Inc.	TRAZODONE HYDROCHLORIDE	150 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (57664-053-74)