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=ANDA077510"
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
60687-715-21 60687-715 HUMAN PRESCRIPTION DRUG Colestipol Hydrochloride Colestipol Hydrochloride TABLET, FILM COATED ORAL 20230510 N/A ANDA ANDA077510 American Health Packaging COLESTIPOL HYDROCHLORIDE 1 g/1 30 BLISTER PACK in 1 CARTON (60687-715-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-715-11)
0115-2142-02 0115-2142 HUMAN PRESCRIPTION DRUG COLESTIPOL HYDROCHLORIDE COLESTIPOL HYDROCHLORIDE TABLET, FILM COATED ORAL 20210817 20241231 ANDA ANDA077510 Amneal Pharmaceuticals of New York LLC COLESTIPOL HYDROCHLORIDE 1 g/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0115-2142-02)
0115-2142-16 0115-2142 HUMAN PRESCRIPTION DRUG COLESTIPOL HYDROCHLORIDE COLESTIPOL HYDROCHLORIDE TABLET, FILM COATED ORAL 20210817 20241231 ANDA ANDA077510 Amneal Pharmaceuticals of New York LLC COLESTIPOL HYDROCHLORIDE 1 g/1 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0115-2142-16)
0115-5211-02 0115-5211 HUMAN PRESCRIPTION DRUG COLESTIPOL HYDROCHLORIDE COLESTIPOL HYDROCHLORIDE TABLET, FILM COATED ORAL 20210817 N/A ANDA ANDA077510 Amneal Pharmaceuticals of New York LLC COLESTIPOL HYDROCHLORIDE 1 g/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0115-5211-02)
0115-5211-16 0115-5211 HUMAN PRESCRIPTION DRUG COLESTIPOL HYDROCHLORIDE COLESTIPOL HYDROCHLORIDE TABLET, FILM COATED ORAL 20210817 N/A ANDA ANDA077510 Amneal Pharmaceuticals of New York LLC COLESTIPOL HYDROCHLORIDE 1 g/1 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0115-5211-16)
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