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=ANDA077336"
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
71610-441-53 71610-441 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200624 N/A ANDA ANDA077336 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 750 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-441-53)
68788-8532-1 68788-8532 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20231003 N/A ANDA ANDA077336 Preferred Pharmaceuticals Inc. METFORMIN HYDROCHLORIDE 750 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8532-1)
62756-143-01 62756-143 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20060209 N/A ANDA ANDA077336 Sun Pharmaceutical Industries, Inc. METFORMIN HYDROCHLORIDE 750 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-143-01)
71610-447-30 71610-447 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200724 N/A ANDA ANDA077336 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 500 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-447-30)
71610-447-53 71610-447 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200724 N/A ANDA ANDA077336 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 500 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-447-53)
71610-447-60 71610-447 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200724 N/A ANDA ANDA077336 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 500 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-447-60)
71610-447-70 71610-447 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200724 N/A ANDA ANDA077336 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 500 mg/1 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-447-70)
71610-447-80 71610-447 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200724 N/A ANDA ANDA077336 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 500 mg/1 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-447-80)
71610-447-94 71610-447 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20210311 N/A ANDA ANDA077336 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 500 mg/1 360 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-447-94)
62756-142-01 62756-142 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20060209 N/A ANDA ANDA077336 Sun Pharmaceutical Industries, Inc. METFORMIN HYDROCHLORIDE 500 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-142-01)
62756-142-02 62756-142 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20060209 N/A ANDA ANDA077336 Sun Pharmaceutical Industries, Inc. METFORMIN HYDROCHLORIDE 500 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-142-02)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase