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
71205-401-60	71205-401	HUMAN PRESCRIPTION DRUG	Quetiapine	Quetiapine	TABLET, FILM COATED	ORAL	20200213	N/A	ANDA	ANDA202152	Proficient Rx LP	QUETIAPINE FUMARATE	200 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-401-60)
71205-401-90	71205-401	HUMAN PRESCRIPTION DRUG	Quetiapine	Quetiapine	TABLET, FILM COATED	ORAL	20200213	N/A	ANDA	ANDA202152	Proficient Rx LP	QUETIAPINE FUMARATE	200 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-401-90)
63629-7116-1	63629-7116	HUMAN PRESCRIPTION DRUG	Quetiapine	Quetiapine	TABLET, FILM COATED	ORAL	20161017	N/A	ANDA	ANDA202152	Bryant Ranch Prepack	QUETIAPINE FUMARATE	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63629-7116-1)
63629-7116-2	63629-7116	HUMAN PRESCRIPTION DRUG	Quetiapine	Quetiapine	TABLET, FILM COATED	ORAL	20240808	N/A	ANDA	ANDA202152	Bryant Ranch Prepack	QUETIAPINE FUMARATE	400 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (63629-7116-2)
63629-7116-3	63629-7116	HUMAN PRESCRIPTION DRUG	Quetiapine	Quetiapine	TABLET, FILM COATED	ORAL	20170919	N/A	ANDA	ANDA202152	Bryant Ranch Prepack	QUETIAPINE FUMARATE	400 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63629-7116-3)
63629-7116-4	63629-7116	HUMAN PRESCRIPTION DRUG	Quetiapine	Quetiapine	TABLET, FILM COATED	ORAL	20171218	N/A	ANDA	ANDA202152	Bryant Ranch Prepack	QUETIAPINE FUMARATE	400 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (63629-7116-4)
63629-7116-5	63629-7116	HUMAN PRESCRIPTION DRUG	Quetiapine	Quetiapine	TABLET, FILM COATED	ORAL	20240808	N/A	ANDA	ANDA202152	Bryant Ranch Prepack	QUETIAPINE FUMARATE	400 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63629-7116-5)