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=ANDA216208"
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
59651-514-03 59651-514 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET, ORALLY DISINTEGRATING ORAL 20260218 N/A ANDA ANDA216208 Aurobindo Pharma Limited ARIPIPRAZOLE 10 mg/1 3 BLISTER PACK in 1 CARTON (59651-514-03) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
59651-514-30 59651-514 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET, ORALLY DISINTEGRATING ORAL 20260218 N/A ANDA ANDA216208 Aurobindo Pharma Limited ARIPIPRAZOLE 10 mg/1 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (59651-514-30)
59651-515-03 59651-515 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET, ORALLY DISINTEGRATING ORAL 20260218 N/A ANDA ANDA216208 Aurobindo Pharma Limited ARIPIPRAZOLE 15 mg/1 3 BLISTER PACK in 1 CARTON (59651-515-03) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
59651-515-30 59651-515 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET, ORALLY DISINTEGRATING ORAL 20260218 N/A ANDA ANDA216208 Aurobindo Pharma Limited ARIPIPRAZOLE 15 mg/1 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (59651-515-30)
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