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=ANDA215629"
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
69025-133-01 69025-133 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20211130 N/A ANDA ANDA215629 Aizant Drug Research Solutions PVT LTD METFORMIN HYDROCHLORIDE 1000 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69025-133-01)
72664-227-01 72664-227 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20211130 N/A ANDA ANDA215629 VGYAAN Pharmaceuticals LLC METFORMIN HYDROCHLORIDE 500 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72664-227-01)
72664-228-90 72664-228 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20211130 N/A ANDA ANDA215629 VGYAAN Pharmaceuticals LLC METFORMIN HYDROCHLORIDE 1000 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72664-228-90)
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