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=ANDA205981"
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
0378-8175-93 0378-8175 HUMAN PRESCRIPTION DRUG Saxagliptin and Metformin saxagliptin and metformin TABLET, FILM COATED, EXTENDED RELEASE ORAL 20230808 N/A ANDA ANDA205981 Mylan Pharmaceuticals Inc. METFORMIN HYDROCHLORIDE; SAXAGLIPTIN HYDROCHLORIDE DIHYDRATE 500 mg/1; 5 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-8175-93)
0378-8176-91 0378-8176 HUMAN PRESCRIPTION DRUG Saxagliptin and Metformin saxagliptin and metformin TABLET, FILM COATED, EXTENDED RELEASE ORAL 20230808 N/A ANDA ANDA205981 Mylan Pharmaceuticals Inc. METFORMIN HYDROCHLORIDE; SAXAGLIPTIN HYDROCHLORIDE DIHYDRATE 1000 mg/1; 2.5 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-8176-91)
0378-8177-93 0378-8177 HUMAN PRESCRIPTION DRUG Saxagliptin and Metformin saxagliptin and metformin TABLET, FILM COATED, EXTENDED RELEASE ORAL 20230808 N/A ANDA ANDA205981 Mylan Pharmaceuticals Inc. METFORMIN HYDROCHLORIDE; SAXAGLIPTIN HYDROCHLORIDE DIHYDRATE 1000 mg/1; 5 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-8177-93)
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