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
59651-412-30	59651-412	HUMAN PRESCRIPTION DRUG	DEFERASIROX	DEFERASIROX	TABLET, FILM COATED	ORAL	20231016	N/A	ANDA	ANDA214474	Aurobindo Pharma Limited	DEFERASIROX	360 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (59651-412-30)
59651-411-30	59651-411	HUMAN PRESCRIPTION DRUG	DEFERASIROX	DEFERASIROX	TABLET, FILM COATED	ORAL	20231016	N/A	ANDA	ANDA214474	Aurobindo Pharma Limited	DEFERASIROX	180 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (59651-411-30)
59651-410-30	59651-410	HUMAN PRESCRIPTION DRUG	DEFERASIROX	DEFERASIROX	TABLET, FILM COATED	ORAL	20231016	N/A	ANDA	ANDA214474	Aurobindo Pharma Limited	DEFERASIROX	90 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (59651-410-30)
72603-231-01	72603-231	HUMAN PRESCRIPTION DRUG	DEFERASIROX	DEFERASIROX	TABLET, FILM COATED	ORAL	20231016	N/A	ANDA	ANDA214474	NorthStar Rx LLC	DEFERASIROX	90 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72603-231-01)
72603-232-01	72603-232	HUMAN PRESCRIPTION DRUG	DEFERASIROX	DEFERASIROX	TABLET, FILM COATED	ORAL	20231016	N/A	ANDA	ANDA214474	NorthStar Rx LLC	DEFERASIROX	180 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72603-232-01)
72603-233-01	72603-233	HUMAN PRESCRIPTION DRUG	DEFERASIROX	DEFERASIROX	TABLET, FILM COATED	ORAL	20231016	N/A	ANDA	ANDA214474	NorthStar Rx LLC	DEFERASIROX	360 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72603-233-01)