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=ANDA209236"
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
59651-018-05 59651-018 HUMAN PRESCRIPTION DRUG Niacin Niacin TABLET, EXTENDED RELEASE ORAL 20180201 N/A ANDA ANDA209236 Aurobindo Pharma Limited NIACIN 500 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-018-05)
59651-018-18 59651-018 HUMAN PRESCRIPTION DRUG Niacin Niacin TABLET, EXTENDED RELEASE ORAL 20180201 N/A ANDA ANDA209236 Aurobindo Pharma Limited NIACIN 500 mg/1 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-018-18)
59651-018-90 59651-018 HUMAN PRESCRIPTION DRUG Niacin Niacin TABLET, EXTENDED RELEASE ORAL 20180201 N/A ANDA ANDA209236 Aurobindo Pharma Limited NIACIN 500 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-018-90)
59651-020-05 59651-020 HUMAN PRESCRIPTION DRUG Niacin Niacin TABLET, EXTENDED RELEASE ORAL 20180201 N/A ANDA ANDA209236 Aurobindo Pharma Limited NIACIN 1000 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-020-05)
59651-020-18 59651-020 HUMAN PRESCRIPTION DRUG Niacin Niacin TABLET, EXTENDED RELEASE ORAL 20180201 N/A ANDA ANDA209236 Aurobindo Pharma Limited NIACIN 1000 mg/1 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-020-18)
59651-020-90 59651-020 HUMAN PRESCRIPTION DRUG Niacin Niacin TABLET, EXTENDED RELEASE ORAL 20180201 N/A ANDA ANDA209236 Aurobindo Pharma Limited NIACIN 1000 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-020-90)
59651-019-05 59651-019 HUMAN PRESCRIPTION DRUG Niacin Niacin TABLET, EXTENDED RELEASE ORAL 20180201 N/A ANDA ANDA209236 Aurobindo Pharma Limited NIACIN 750 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-019-05)
59651-019-18 59651-019 HUMAN PRESCRIPTION DRUG Niacin Niacin TABLET, EXTENDED RELEASE ORAL 20180201 N/A ANDA ANDA209236 Aurobindo Pharma Limited NIACIN 750 mg/1 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-019-18)
59651-019-90 59651-019 HUMAN PRESCRIPTION DRUG Niacin Niacin TABLET, EXTENDED RELEASE ORAL 20180201 N/A ANDA ANDA209236 Aurobindo Pharma Limited NIACIN 750 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-019-90)
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