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=ANDA202917"
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
47335-306-18 47335-306 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180522 N/A ANDA ANDA202917 Sun Pharmaceutical Industries, Inc. METFORMIN HYDROCHLORIDE 1000 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-306-18)
47335-306-81 47335-306 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20190722 N/A ANDA ANDA202917 Sun Pharmaceutical Industries, Inc. METFORMIN HYDROCHLORIDE 1000 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-306-81)
47335-305-88 47335-305 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180522 N/A ANDA ANDA202917 Sun Pharmaceutical Industries, Inc. METFORMIN HYDROCHLORIDE 500 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-305-88)
47335-305-83 47335-305 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180522 N/A ANDA ANDA202917 Sun Pharmaceutical Industries, Inc. METFORMIN HYDROCHLORIDE 500 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-305-83)
47335-305-18 47335-305 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180522 N/A ANDA ANDA202917 Sun Pharmaceutical Industries, Inc. METFORMIN HYDROCHLORIDE 500 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-305-18)
47335-306-83 47335-306 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180522 N/A ANDA ANDA202917 Sun Pharmaceutical Industries, Inc. METFORMIN HYDROCHLORIDE 1000 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-306-83)
47335-306-88 47335-306 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180522 N/A ANDA ANDA202917 Sun Pharmaceutical Industries, Inc. METFORMIN HYDROCHLORIDE 1000 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-306-88)
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