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=ANDA090692"
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
68788-8520-6 68788-8520 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, EXTENDED RELEASE ORAL 20230901 N/A ANDA ANDA090692 Preferred Pharmaceuticals, Inc. METFORMIN HYDROCHLORIDE 1000 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8520-6)
68180-336-07 68180-336 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, EXTENDED RELEASE ORAL 20110930 N/A ANDA ANDA090692 Lupin Pharmaceuticals, Inc. METFORMIN HYDROCHLORIDE 500 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-336-07)
68180-337-07 68180-337 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, EXTENDED RELEASE ORAL 20110930 N/A ANDA ANDA090692 Lupin Pharmaceuticals, Inc. METFORMIN HYDROCHLORIDE 1000 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-337-07)
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