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
68788-7186-6	68788-7186	HUMAN PRESCRIPTION DRUG	Quetiapine	Quetiapine	TABLET, FILM COATED	ORAL	20180614	N/A	ANDA	ANDA202152	Preferred Pharmaceuticals Inc.	QUETIAPINE FUMARATE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-7186-6)
68788-7186-8	68788-7186	HUMAN PRESCRIPTION DRUG	Quetiapine	Quetiapine	TABLET, FILM COATED	ORAL	20180614	N/A	ANDA	ANDA202152	Preferred Pharmaceuticals Inc.	QUETIAPINE FUMARATE	50 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (68788-7186-8)
68788-7186-9	68788-7186	HUMAN PRESCRIPTION DRUG	Quetiapine	Quetiapine	TABLET, FILM COATED	ORAL	20180614	N/A	ANDA	ANDA202152	Preferred Pharmaceuticals Inc.	QUETIAPINE FUMARATE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-7186-9)
72789-255-60	72789-255	HUMAN PRESCRIPTION DRUG	Quetiapine	Quetiapine	TABLET, FILM COATED	ORAL	20220628	N/A	ANDA	ANDA202152	PD-Rx Pharmaceuticals, Inc.	QUETIAPINE FUMARATE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-255-60)
80425-0107-3	80425-0107	HUMAN PRESCRIPTION DRUG	Quetiapine	Quetiapine	TABLET, FILM COATED	ORAL	20151201	N/A	ANDA	ANDA202152	Advanced Rx Pharmacy of Tennessee, LLC	QUETIAPINE FUMARATE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (80425-0107-3)
80425-0143-3	80425-0143	HUMAN PRESCRIPTION DRUG	Quetiapine	Quetiapine	TABLET, FILM COATED	ORAL	20151201	N/A	ANDA	ANDA202152	Advanced Rx Pharmacy of Tennessee, LLC	QUETIAPINE FUMARATE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (80425-0143-3)