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)
检索条件:" 注册申请号=ANDA215223"
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
70771-1653-5 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)
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)
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