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"
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
71093-132-04 71093-132 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET ORAL 20180115 N/A ANDA ANDA203769 ACI Healthcare USA, Inc. METFORMIN HYDROCHLORIDE 500 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (71093-132-04)
71093-132-05 71093-132 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET ORAL 20180115 N/A ANDA ANDA203769 ACI Healthcare USA, Inc. METFORMIN HYDROCHLORIDE 500 mg/1 500 TABLET in 1 BOTTLE, PLASTIC (71093-132-05)
71093-132-06 71093-132 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET ORAL 20180115 N/A ANDA ANDA203769 ACI Healthcare USA, Inc. METFORMIN HYDROCHLORIDE 500 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (71093-132-06)
71093-133-04 71093-133 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET ORAL 20180115 N/A ANDA ANDA203769 ACI Healthcare USA, Inc. METFORMIN HYDROCHLORIDE 850 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (71093-133-04)
71093-133-05 71093-133 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET ORAL 20180115 N/A ANDA ANDA203769 ACI Healthcare USA, Inc. METFORMIN HYDROCHLORIDE 850 mg/1 500 TABLET in 1 BOTTLE, PLASTIC (71093-133-05)
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)
69367-180-05 69367-180 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride METFORMIN HYDROCHLORIDE TABLET, FILM COATED ORAL 20171121 N/A ANDA ANDA203769 Westminster Pharmaceuticals, LLC METFORMIN HYDROCHLORIDE 500 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-180-05)
69367-180-10 69367-180 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride METFORMIN HYDROCHLORIDE TABLET, FILM COATED ORAL 20200421 N/A ANDA ANDA203769 Westminster Pharmaceuticals, LLC METFORMIN HYDROCHLORIDE 500 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-180-10)
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)
72162-1522-1 72162-1522 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET ORAL 20240205 N/A ANDA ANDA203769 Bryant Ranch Prepack METFORMIN HYDROCHLORIDE 500 mg/1 100 TABLET in 1 BOTTLE (72162-1522-1)
72162-1522-5 72162-1522 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET ORAL 20240205 N/A ANDA ANDA203769 Bryant Ranch Prepack METFORMIN HYDROCHLORIDE 500 mg/1 500 TABLET in 1 BOTTLE (72162-1522-5)
72162-1523-1 72162-1523 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET ORAL 20240205 N/A ANDA ANDA203769 Bryant Ranch Prepack METFORMIN HYDROCHLORIDE 1000 mg/1 100 TABLET in 1 BOTTLE (72162-1523-1)
72162-1523-5 72162-1523 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET ORAL 20240205 N/A ANDA ANDA203769 Bryant Ranch Prepack METFORMIN HYDROCHLORIDE 1000 mg/1 500 TABLET in 1 BOTTLE (72162-1523-5)
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