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=ANDA205096"
符合检索条件的记录共 73 条，共 4 页，当前第 2 页 ，可点击列名称排序
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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
71335-1303-5 71335-1303 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, COATED ORAL 20190821 N/A ANDA ANDA205096 Bryant Ranch Prepack METFORMIN HYDROCHLORIDE 500 mg/1 90 TABLET, COATED in 1 BOTTLE (71335-1303-5)
71335-1303-6 71335-1303 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, COATED ORAL 20190821 N/A ANDA ANDA205096 Bryant Ranch Prepack METFORMIN HYDROCHLORIDE 500 mg/1 28 TABLET, COATED in 1 BOTTLE (71335-1303-6)
71335-1303-7 71335-1303 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, COATED ORAL 20190821 N/A ANDA ANDA205096 Bryant Ranch Prepack METFORMIN HYDROCHLORIDE 500 mg/1 56 TABLET, COATED in 1 BOTTLE (71335-1303-7)
71335-1303-8 71335-1303 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, COATED ORAL 20190821 N/A ANDA ANDA205096 Bryant Ranch Prepack METFORMIN HYDROCHLORIDE 500 mg/1 180 TABLET, COATED in 1 BOTTLE (71335-1303-8)
71335-1303-9 71335-1303 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, COATED ORAL 20190821 N/A ANDA ANDA205096 Bryant Ranch Prepack METFORMIN HYDROCHLORIDE 500 mg/1 10 TABLET, COATED in 1 BOTTLE (71335-1303-9)
51224-020-50 51224-020 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, COATED ORAL 20190501 N/A ANDA ANDA205096 TAGI Pharma, Inc. METFORMIN HYDROCHLORIDE 500 mg/1 100 TABLET, COATED in 1 BOTTLE (51224-020-50)
51224-020-60 51224-020 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, COATED ORAL 20190501 N/A ANDA ANDA205096 TAGI Pharma, Inc. METFORMIN HYDROCHLORIDE 500 mg/1 500 TABLET, COATED in 1 BOTTLE (51224-020-60)
51224-020-70 51224-020 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, COATED ORAL 20190501 N/A ANDA ANDA205096 TAGI Pharma, Inc. METFORMIN HYDROCHLORIDE 500 mg/1 1000 TABLET, COATED in 1 BOTTLE (51224-020-70)
51224-120-50 51224-120 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, COATED ORAL 20190501 N/A ANDA ANDA205096 TAGI Pharma, Inc. METFORMIN HYDROCHLORIDE 850 mg/1 100 TABLET, COATED in 1 BOTTLE (51224-120-50)
51224-120-60 51224-120 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, COATED ORAL 20190501 N/A ANDA ANDA205096 TAGI Pharma, Inc. METFORMIN HYDROCHLORIDE 850 mg/1 500 TABLET, COATED in 1 BOTTLE (51224-120-60)
51224-120-70 51224-120 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, COATED ORAL 20190501 N/A ANDA ANDA205096 TAGI Pharma, Inc. METFORMIN HYDROCHLORIDE 850 mg/1 1000 TABLET, COATED in 1 BOTTLE (51224-120-70)
51224-220-50 51224-220 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, COATED ORAL 20190501 N/A ANDA ANDA205096 TAGI Pharma, Inc. METFORMIN HYDROCHLORIDE 1000 mg/1 100 TABLET, COATED in 1 BOTTLE (51224-220-50)
51224-220-60 51224-220 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, COATED ORAL 20190501 N/A ANDA ANDA205096 TAGI Pharma, Inc. METFORMIN HYDROCHLORIDE 1000 mg/1 500 TABLET, COATED in 1 BOTTLE (51224-220-60)
51224-220-70 51224-220 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, COATED ORAL 20190501 N/A ANDA ANDA205096 TAGI Pharma, Inc. METFORMIN HYDROCHLORIDE 1000 mg/1 1000 TABLET, COATED in 1 BOTTLE (51224-220-70)
83301-0008-1 83301-0008 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, COATED ORAL 20240101 N/A ANDA ANDA205096 Mullan Pharmaceutical Inc. METFORMIN HYDROCHLORIDE 500 mg/1 100 TABLET, COATED in 1 BOTTLE (83301-0008-1)
83301-0008-2 83301-0008 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, COATED ORAL 20240101 N/A ANDA ANDA205096 Mullan Pharmaceutical Inc. METFORMIN HYDROCHLORIDE 500 mg/1 500 TABLET, COATED in 1 BOTTLE (83301-0008-2)
83301-0008-3 83301-0008 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, COATED ORAL 20240101 N/A ANDA ANDA205096 Mullan Pharmaceutical Inc. METFORMIN HYDROCHLORIDE 500 mg/1 1000 TABLET, COATED in 1 BOTTLE (83301-0008-3)
83301-0009-1 83301-0009 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, COATED ORAL 20240101 N/A ANDA ANDA205096 Mullan Pharmaceutical Inc. METFORMIN HYDROCHLORIDE 850 mg/1 100 TABLET, COATED in 1 BOTTLE (83301-0009-1)
83301-0009-2 83301-0009 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, COATED ORAL 20240101 N/A ANDA ANDA205096 Mullan Pharmaceutical Inc. METFORMIN HYDROCHLORIDE 850 mg/1 500 TABLET, COATED in 1 BOTTLE (83301-0009-2)
83301-0009-3 83301-0009 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, COATED ORAL 20240101 N/A ANDA ANDA205096 Mullan Pharmaceutical Inc. METFORMIN HYDROCHLORIDE 850 mg/1 1000 TABLET, COATED in 1 BOTTLE (83301-0009-3)
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