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=ANDA209882"
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
68788-8756-9 68788-8756 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20241014 N/A ANDA ANDA209882 Preferred Pharmaceuticals Inc. METFORMIN HYDROCHLORIDE 850 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-8756-9)
71335-2593-5 71335-2593 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20250604 N/A ANDA ANDA209882 Bryant Ranch Prepack METFORMIN HYDROCHLORIDE 850 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-2593-5)
71335-2593-6 71335-2593 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20250604 N/A ANDA ANDA209882 Bryant Ranch Prepack METFORMIN HYDROCHLORIDE 850 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71335-2593-6)
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