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
67877-552-90	67877-552	HUMAN PRESCRIPTION DRUG	Deferasirox	Deferasirox	TABLET, FILM COATED	ORAL	20200401	N/A	ANDA	ANDA210555	Ascend Laboratories, LLC	DEFERASIROX	90 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (67877-552-90)
67877-553-30	67877-553	HUMAN PRESCRIPTION DRUG	Deferasirox	Deferasirox	TABLET, FILM COATED	ORAL	20200704	N/A	ANDA	ANDA210555	Ascend Laboratories, LLC	DEFERASIROX	180 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67877-553-30)
67877-553-90	67877-553	HUMAN PRESCRIPTION DRUG	Deferasirox	Deferasirox	TABLET, FILM COATED	ORAL	20200704	N/A	ANDA	ANDA210555	Ascend Laboratories, LLC	DEFERASIROX	180 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (67877-553-90)
67877-554-30	67877-554	HUMAN PRESCRIPTION DRUG	Deferasirox	Deferasirox	TABLET, FILM COATED	ORAL	20200401	N/A	ANDA	ANDA210555	Ascend Laboratories, LLC	DEFERASIROX	360 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67877-554-30)
67877-554-90	67877-554	HUMAN PRESCRIPTION DRUG	Deferasirox	Deferasirox	TABLET, FILM COATED	ORAL	20200401	N/A	ANDA	ANDA210555	Ascend Laboratories, LLC	DEFERASIROX	360 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (67877-554-90)
67877-552-30	67877-552	HUMAN PRESCRIPTION DRUG	Deferasirox	Deferasirox	TABLET, FILM COATED	ORAL	20200401	N/A	ANDA	ANDA210555	Ascend Laboratories, LLC	DEFERASIROX	90 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67877-552-30)