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
68475-010-01	68475-010	HUMAN PRESCRIPTION DRUG	Sevelamer carbonate	Sevelamer carbonate	TABLET, FILM COATED	ORAL	20251101	N/A	ANDA	ANDA219931	Navinta LLC	SEVELAMER CARBONATE	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68475-010-01)
68475-010-02	68475-010	HUMAN PRESCRIPTION DRUG	Sevelamer carbonate	Sevelamer carbonate	TABLET, FILM COATED	ORAL	20251101	N/A	ANDA	ANDA219931	Navinta LLC	SEVELAMER CARBONATE	800 mg/1	270 TABLET, FILM COATED in 1 BOTTLE (68475-010-02)
68475-010-03	68475-010	HUMAN PRESCRIPTION DRUG	Sevelamer carbonate	Sevelamer carbonate	TABLET, FILM COATED	ORAL	20260102	N/A	ANDA	ANDA219931	Navinta LLC	SEVELAMER CARBONATE	800 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (68475-010-03)
70710-2170-3	70710-2170	HUMAN PRESCRIPTION DRUG	Sevelamer carbonate	Sevelamer carbonate	TABLET, FILM COATED	ORAL	20260401	N/A	ANDA	ANDA219931	Zydus Pharmaceuticals USA Inc.	SEVELAMER CARBONATE	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70710-2170-3)
70710-2170-7	70710-2170	HUMAN PRESCRIPTION DRUG	Sevelamer carbonate	Sevelamer carbonate	TABLET, FILM COATED	ORAL	20260401	N/A	ANDA	ANDA219931	Zydus Pharmaceuticals USA Inc.	SEVELAMER CARBONATE	800 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (70710-2170-7)
70710-2170-8	70710-2170	HUMAN PRESCRIPTION DRUG	Sevelamer carbonate	Sevelamer carbonate	TABLET, FILM COATED	ORAL	20260401	N/A	ANDA	ANDA219931	Zydus Pharmaceuticals USA Inc.	SEVELAMER CARBONATE	800 mg/1	270 TABLET, FILM COATED in 1 BOTTLE (70710-2170-8)