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=ANDA203769"
符合检索条件的记录共 181 条，共 10 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
71335-1834-3 71335-1834 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET ORAL 20210429 N/A ANDA ANDA203769 Bryant Ranch Prepack METFORMIN HYDROCHLORIDE 500 mg/1 100 TABLET in 1 BOTTLE (71335-1834-3)
71610-672-30 71610-672 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET ORAL 20221102 N/A ANDA ANDA203769 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 1000 mg/1 30 TABLET in 1 BOTTLE (71610-672-30)
71610-672-45 71610-672 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET ORAL 20221102 N/A ANDA ANDA203769 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 1000 mg/1 45 TABLET in 1 BOTTLE (71610-672-45)
71610-672-53 71610-672 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET ORAL 20221102 N/A ANDA ANDA203769 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 1000 mg/1 60 TABLET in 1 BOTTLE (71610-672-53)
71610-672-60 71610-672 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET ORAL 20221102 N/A ANDA ANDA203769 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 1000 mg/1 90 TABLET in 1 BOTTLE (71610-672-60)
71610-672-70 71610-672 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET ORAL 20221102 N/A ANDA ANDA203769 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 1000 mg/1 120 TABLET in 1 BOTTLE (71610-672-70)
71610-672-80 71610-672 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET ORAL 20221102 N/A ANDA ANDA203769 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 1000 mg/1 180 TABLET in 1 BOTTLE (71610-672-80)
69367-181-01 69367-181 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride METFORMIN HYDROCHLORIDE TABLET, FILM COATED ORAL 20171121 N/A ANDA ANDA203769 Westminster Pharmaceuticals, LLC METFORMIN HYDROCHLORIDE 850 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-181-01)
69367-181-05 69367-181 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride METFORMIN HYDROCHLORIDE TABLET, FILM COATED ORAL 20171121 N/A ANDA ANDA203769 Westminster Pharmaceuticals, LLC METFORMIN HYDROCHLORIDE 850 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-181-05)
71093-134-04 71093-134 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET ORAL 20180115 N/A ANDA ANDA203769 ACI Healthcare USA, Inc. METFORMIN HYDROCHLORIDE 1000 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (71093-134-04)
71093-134-05 71093-134 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET ORAL 20180115 N/A ANDA ANDA203769 ACI Healthcare USA, Inc. METFORMIN HYDROCHLORIDE 1000 mg/1 500 TABLET in 1 BOTTLE, PLASTIC (71093-134-05)
50228-105-00 50228-105 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET ORAL 20150201 N/A ANDA ANDA203769 ScieGen Pharmaceuticals Inc METFORMIN HYDROCHLORIDE 500 mg/1 9000 TABLET in 1 BOTTLE (50228-105-00)
50228-105-01 50228-105 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET ORAL 20150201 N/A ANDA ANDA203769 ScieGen Pharmaceuticals Inc METFORMIN HYDROCHLORIDE 500 mg/1 100 TABLET in 1 BOTTLE (50228-105-01)
50228-105-05 50228-105 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET ORAL 20150201 N/A ANDA ANDA203769 ScieGen Pharmaceuticals Inc METFORMIN HYDROCHLORIDE 500 mg/1 500 TABLET in 1 BOTTLE (50228-105-05)
50228-105-10 50228-105 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET ORAL 20150201 N/A ANDA ANDA203769 ScieGen Pharmaceuticals Inc METFORMIN HYDROCHLORIDE 500 mg/1 1000 TABLET in 1 BOTTLE (50228-105-10)
50228-105-30 50228-105 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET ORAL 20150201 N/A ANDA ANDA203769 ScieGen Pharmaceuticals Inc METFORMIN HYDROCHLORIDE 500 mg/1 30 TABLET in 1 BOTTLE (50228-105-30)
69367-182-01 69367-182 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride METFORMIN HYDROCHLORIDE TABLET, FILM COATED ORAL 20171121 N/A ANDA ANDA203769 Westminster Pharmaceuticals, LLC METFORMIN HYDROCHLORIDE 1000 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-182-01)
69367-182-05 69367-182 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride METFORMIN HYDROCHLORIDE TABLET, FILM COATED ORAL 20171121 N/A ANDA ANDA203769 Westminster Pharmaceuticals, LLC METFORMIN HYDROCHLORIDE 1000 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-182-05)
69367-182-10 69367-182 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride METFORMIN HYDROCHLORIDE TABLET, FILM COATED ORAL 20200421 N/A ANDA ANDA203769 Westminster Pharmaceuticals, LLC METFORMIN HYDROCHLORIDE 1000 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-182-10)
68788-7901-1 68788-7901 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET ORAL 20210514 N/A ANDA ANDA203769 Preferred Pharmaceuticals Inc METFORMIN HYDROCHLORIDE 850 mg/1 100 TABLET in 1 BOTTLE (68788-7901-1)
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