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=ANDA212681"
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
43547-504-09 43547-504 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE metformin hydrochloride TABLET, EXTENDED RELEASE ORAL 20220531 N/A ANDA ANDA212681 Solco Healthcare US, LLC. METFORMIN HYDROCHLORIDE 1000 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (43547-504-09)
43547-504-50 43547-504 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE metformin hydrochloride TABLET, EXTENDED RELEASE ORAL 20220531 N/A ANDA ANDA212681 Solco Healthcare US, LLC. METFORMIN HYDROCHLORIDE 1000 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (43547-504-50)
43547-503-50 43547-503 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE metformin hydrochloride TABLET, EXTENDED RELEASE ORAL 20220531 N/A ANDA ANDA212681 Solco Healthcare US, LLC. METFORMIN HYDROCHLORIDE 500 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (43547-503-50)
43547-503-10 43547-503 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE metformin hydrochloride TABLET, EXTENDED RELEASE ORAL 20220531 N/A ANDA ANDA212681 Solco Healthcare US, LLC. METFORMIN HYDROCHLORIDE 500 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (43547-503-10)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase