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=ANDA078561"
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
0228-4022-11 0228-4022 HUMAN PRESCRIPTION DRUG Alprazolam Alprazolam TABLET, ORALLY DISINTEGRATING ORAL 20100317 N/A ANDA ANDA078561 Actavis Pharma, Inc. ALPRAZOLAM .5 mg/1 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (0228-4022-11)
0228-4024-11 0228-4024 HUMAN PRESCRIPTION DRUG Alprazolam Alprazolam TABLET, ORALLY DISINTEGRATING ORAL 20100317 N/A ANDA ANDA078561 Actavis Pharma, Inc. ALPRAZOLAM 1 mg/1 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (0228-4024-11)
0228-4025-11 0228-4025 HUMAN PRESCRIPTION DRUG Alprazolam Alprazolam TABLET, ORALLY DISINTEGRATING ORAL 20100317 N/A ANDA ANDA078561 Actavis Pharma, Inc. ALPRAZOLAM 2 mg/1 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (0228-4025-11)
0228-4019-11 0228-4019 HUMAN PRESCRIPTION DRUG Alprazolam Alprazolam TABLET, ORALLY DISINTEGRATING ORAL 20100317 N/A ANDA ANDA078561 Actavis Pharma, Inc. ALPRAZOLAM .25 mg/1 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (0228-4019-11)
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