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
72865-268-05	72865-268	HUMAN PRESCRIPTION DRUG	Quetiapine Fumarate	Quetiapine Fumarate	TABLET, FILM COATED	ORAL	20240202	N/A	ANDA	ANDA204316	XLCare Pharmaceuticals Inc.	QUETIAPINE FUMARATE	300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72865-268-05)
72865-268-60	72865-268	HUMAN PRESCRIPTION DRUG	Quetiapine Fumarate	Quetiapine Fumarate	TABLET, FILM COATED	ORAL	20240202	N/A	ANDA	ANDA204316	XLCare Pharmaceuticals Inc.	QUETIAPINE FUMARATE	300 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72865-268-60)
72865-269-01	72865-269	HUMAN PRESCRIPTION DRUG	Quetiapine Fumarate	Quetiapine Fumarate	TABLET, FILM COATED	ORAL	20240202	N/A	ANDA	ANDA204316	XLCare Pharmaceuticals Inc.	QUETIAPINE FUMARATE	400 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72865-269-01)
72865-269-05	72865-269	HUMAN PRESCRIPTION DRUG	Quetiapine Fumarate	Quetiapine Fumarate	TABLET, FILM COATED	ORAL	20240202	N/A	ANDA	ANDA204316	XLCare Pharmaceuticals Inc.	QUETIAPINE FUMARATE	400 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72865-269-05)
72865-269-90	72865-269	HUMAN PRESCRIPTION DRUG	Quetiapine Fumarate	Quetiapine Fumarate	TABLET, FILM COATED	ORAL	20240722	N/A	ANDA	ANDA204316	XLCare Pharmaceuticals Inc.	QUETIAPINE FUMARATE	400 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72865-269-90)
60760-764-30	60760-764	HUMAN PRESCRIPTION DRUG	Quetiapine Fumarate	Quetiapine Fumarate	TABLET, FILM COATED	ORAL	20250521	N/A	ANDA	ANDA204316	ST. MARY'S MEDICAL PARK PHARMACY	QUETIAPINE FUMARATE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-764-30)