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
70710-1467-5	70710-1467	HUMAN PRESCRIPTION DRUG	Colestipol hydrochloride	Colestipol hydrochloride	TABLET, FILM COATED	ORAL	20220504	N/A	ANDA	ANDA215223	Zydus Pharmaceuticals USA Inc.	COLESTIPOL HYDROCHLORIDE	1 g/1	500 TABLET, FILM COATED in 1 BOTTLE (70710-1467-5)
70710-1467-7	70710-1467	HUMAN PRESCRIPTION DRUG	Colestipol hydrochloride	Colestipol hydrochloride	TABLET, FILM COATED	ORAL	20220504	N/A	ANDA	ANDA215223	Zydus Pharmaceuticals USA Inc.	COLESTIPOL HYDROCHLORIDE	1 g/1	120 TABLET, FILM COATED in 1 BOTTLE (70710-1467-7)
70771-1653-5	70771-1653	HUMAN PRESCRIPTION DRUG	Colestipol hydrochloride	Colestipol hydrochloride	TABLET, FILM COATED	ORAL	20220504	N/A	ANDA	ANDA215223	Zydus Lifesciences Limited	COLESTIPOL HYDROCHLORIDE	1 g/1	500 TABLET, FILM COATED in 1 BOTTLE (70771-1653-5)
70771-1653-7	70771-1653	HUMAN PRESCRIPTION DRUG	Colestipol hydrochloride	Colestipol hydrochloride	TABLET, FILM COATED	ORAL	20220504	N/A	ANDA	ANDA215223	Zydus Lifesciences Limited	COLESTIPOL HYDROCHLORIDE	1 g/1	120 TABLET, FILM COATED in 1 BOTTLE (70771-1653-7)