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
33342-241-65	33342-241	HUMAN PRESCRIPTION DRUG	Sevelamer Hydrochloride	Sevelamer Hydrochloride	TABLET, FILM COATED	ORAL	20230526	N/A	ANDA	ANDA206883	Macleods Pharmaceuticals Limited	SEVELAMER HYDROCHLORIDE	400 mg/1	360 TABLET, FILM COATED in 1 BOTTLE (33342-241-65)
33342-242-07	33342-242	HUMAN PRESCRIPTION DRUG	Sevelamer Hydrochloride	Sevelamer Hydrochloride	TABLET, FILM COATED	ORAL	20230526	N/A	ANDA	ANDA206883	Macleods Pharmaceuticals Limited	SEVELAMER HYDROCHLORIDE	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (33342-242-07)
33342-242-57	33342-242	HUMAN PRESCRIPTION DRUG	Sevelamer Hydrochloride	Sevelamer Hydrochloride	TABLET, FILM COATED	ORAL	20230526	N/A	ANDA	ANDA206883	Macleods Pharmaceuticals Limited	SEVELAMER HYDROCHLORIDE	800 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (33342-242-57)