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
0955-1057-30	0955-1057	HUMAN PRESCRIPTION DRUG	Sevelamer Carbonate	Sevelamer Carbonate	TABLET, FILM COATED	ORAL	20230714	N/A	NDA AUTHORIZED GENERIC	NDA022127	Winthrop U.S, a business of sanofi-aventis U.S. LLC	SEVELAMER CARBONATE	800 mg/1	270 TABLET, FILM COATED in 1 BOTTLE (0955-1057-30)
0955-1050-27	0955-1050	HUMAN PRESCRIPTION DRUG	Sevelamer Carbonate	Sevelamer Carbonate	TABLET, FILM COATED	ORAL	20180201	N/A	NDA AUTHORIZED GENERIC	NDA022127	Winthrop U.S, a business of sanofi-aventis U.S. LLC	SEVELAMER CARBONATE	800 mg/1	270 TABLET, FILM COATED in 1 BOTTLE (0955-1050-27)
58468-0133-1	58468-0133	HUMAN PRESCRIPTION DRUG	Renvela	SEVELAMER CARBONATE	TABLET, FILM COATED	ORAL	20230714	N/A	NDA	NDA022127	Genzyme Corporation	SEVELAMER CARBONATE	800 mg/1	270 TABLET, FILM COATED in 1 BOTTLE (58468-0133-1)
58468-0130-1	58468-0130	HUMAN PRESCRIPTION DRUG	Renvela	SEVELAMER CARBONATE	TABLET, FILM COATED	ORAL	20090812	N/A	NDA	NDA022127	Genzyme Corporation	SEVELAMER CARBONATE	800 mg/1	270 TABLET, FILM COATED in 1 BOTTLE (58468-0130-1)