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
31722-013-30	31722-013	HUMAN PRESCRIPTION DRUG	Deferasirox	Deferasirox	TABLET, FILM COATED	ORAL	20210514	N/A	ANDA	ANDA214341	Camber Pharmaceuticals, Inc.	DEFERASIROX	360 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (31722-013-30)
31722-012-30	31722-012	HUMAN PRESCRIPTION DRUG	Deferasirox	Deferasirox	TABLET, FILM COATED	ORAL	20210514	N/A	ANDA	ANDA214341	Camber Pharmaceuticals, Inc.	DEFERASIROX	180 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (31722-012-30)
31722-011-30	31722-011	HUMAN PRESCRIPTION DRUG	Deferasirox	Deferasirox	TABLET, FILM COATED	ORAL	20210514	N/A	ANDA	ANDA214341	Camber Pharmaceuticals, Inc.	DEFERASIROX	90 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (31722-011-30)