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
70771-1520-0	70771-1520	HUMAN PRESCRIPTION DRUG	Sevelamer carbonate	Sevelamer carbonate	TABLET, FILM COATED	ORAL	20200917	N/A	ANDA	ANDA207759	Zydus Lifesciences Limited	SEVELAMER CARBONATE	800 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (70771-1520-0)
70771-1520-4	70771-1520	HUMAN PRESCRIPTION DRUG	Sevelamer carbonate	Sevelamer carbonate	TABLET, FILM COATED	ORAL	20200917	N/A	ANDA	ANDA207759	Zydus Lifesciences Limited	SEVELAMER CARBONATE	800 mg/1	10 BLISTER PACK in 1 CARTON (70771-1520-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1520-2)
70771-1520-8	70771-1520	HUMAN PRESCRIPTION DRUG	Sevelamer carbonate	Sevelamer carbonate	TABLET, FILM COATED	ORAL	20200917	N/A	ANDA	ANDA207759	Zydus Lifesciences Limited	SEVELAMER CARBONATE	800 mg/1	270 TABLET, FILM COATED in 1 BOTTLE (70771-1520-8)
68382-824-10	68382-824	HUMAN PRESCRIPTION DRUG	Sevelamer carbonate	Sevelamer carbonate	TABLET, FILM COATED	ORAL	20200917	N/A	ANDA	ANDA207759	Zydus Pharmaceuticals USA Inc.	SEVELAMER CARBONATE	800 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68382-824-10)
68382-824-27	68382-824	HUMAN PRESCRIPTION DRUG	Sevelamer carbonate	Sevelamer carbonate	TABLET, FILM COATED	ORAL	20200917	N/A	ANDA	ANDA207759	Zydus Pharmaceuticals USA Inc.	SEVELAMER CARBONATE	800 mg/1	270 TABLET, FILM COATED in 1 BOTTLE (68382-824-27)
68382-824-77	68382-824	HUMAN PRESCRIPTION DRUG	Sevelamer carbonate	Sevelamer carbonate	TABLET, FILM COATED	ORAL	20200917	N/A	ANDA	ANDA207759	Zydus Pharmaceuticals USA Inc.	SEVELAMER CARBONATE	800 mg/1	10 BLISTER PACK in 1 CARTON (68382-824-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68382-824-30)