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
69097-893-93	69097-893	HUMAN PRESCRIPTION DRUG	Sevelamer carbonate	SEVELAMER CARBONATE	TABLET, FILM COATED	ORAL	20171026	N/A	ANDA	ANDA203860	Cipla USA Inc.	SEVELAMER CARBONATE	800 mg/1	270 TABLET, FILM COATED in 1 BOTTLE (69097-893-93)
69097-967-93	69097-967	HUMAN PRESCRIPTION DRUG	Sevelamer carbonate	SEVELAMER CARBONATE	TABLET, FILM COATED	ORAL	20190808	N/A	ANDA	ANDA203860	Cipla USA Inc.	SEVELAMER CARBONATE	800 mg/1	270 TABLET, FILM COATED in 1 BOTTLE (69097-967-93)
76282-664-27	76282-664	HUMAN PRESCRIPTION DRUG	Sevelamer carbonate	SEVELAMER CARBONATE	TABLET, FILM COATED	ORAL	20190808	N/A	ANDA	ANDA203860	Exelan Pharmaceuticals Inc.	SEVELAMER CARBONATE	800 mg/1	270 TABLET, FILM COATED in 1 BOTTLE (76282-664-27)
76282-407-27	76282-407	HUMAN PRESCRIPTION DRUG	Sevelamer carbonate	SEVELAMER CARBONATE	TABLET, FILM COATED	ORAL	20171108	N/A	ANDA	ANDA203860	Exelan Pharmaceuticals Inc.	SEVELAMER CARBONATE	800 mg/1	270 TABLET, FILM COATED in 1 BOTTLE (76282-407-27)