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
60687-449-01	60687-449	HUMAN PRESCRIPTION DRUG	Sevelamer Hydrochloride	Sevelamer Hydrochloride	TABLET, FILM COATED	ORAL	20191001	N/A	ANDA	ANDA204724	American Health Packaging	SEVELAMER HYDROCHLORIDE	800 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-449-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-449-11)
68462-446-26	68462-446	HUMAN PRESCRIPTION DRUG	sevelamer hydrochloride	sevelamer hydrochloride	TABLET, FILM COATED	ORAL	20190208	N/A	ANDA	ANDA204724	Glenmark Pharmaceuticals Inc., USA	SEVELAMER HYDROCHLORIDE	400 mg/1	360 TABLET, FILM COATED in 1 BOTTLE (68462-446-26)
68462-446-30	68462-446	HUMAN PRESCRIPTION DRUG	sevelamer hydrochloride	sevelamer hydrochloride	TABLET, FILM COATED	ORAL	20190208	N/A	ANDA	ANDA204724	Glenmark Pharmaceuticals Inc., USA	SEVELAMER HYDROCHLORIDE	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68462-446-30)
68462-447-18	68462-447	HUMAN PRESCRIPTION DRUG	sevelamer hydrochloride	sevelamer hydrochloride	TABLET, FILM COATED	PARENTERAL	20190208	N/A	ANDA	ANDA204724	Glenmark Pharmaceuticals Inc., USA	SEVELAMER HYDROCHLORIDE	800 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (68462-447-18)
68462-447-30	68462-447	HUMAN PRESCRIPTION DRUG	sevelamer hydrochloride	sevelamer hydrochloride	TABLET, FILM COATED	PARENTERAL	20190208	N/A	ANDA	ANDA204724	Glenmark Pharmaceuticals Inc., USA	SEVELAMER HYDROCHLORIDE	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68462-447-30)
72603-148-01	72603-148	HUMAN PRESCRIPTION DRUG	sevelamer hydrochloride	sevelamer hydrochloride	TABLET, FILM COATED	ORAL	20230523	N/A	ANDA	ANDA204724	NorthStar RxLLC	SEVELAMER HYDROCHLORIDE	800 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (72603-148-01)