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=ANDA076921"
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
80425-0305-3 80425-0305 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20230407 N/A ANDA ANDA076921 Advanced Rx Pharmacy of Tennessee, LLC MIRTAZAPINE 15 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (80425-0305-3)
83008-006-60 83008-006 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20230411 N/A ANDA ANDA076921 Quality Care Products, LLC MIRTAZAPINE 15 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (83008-006-60)
83008-006-30 83008-006 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20230523 N/A ANDA ANDA076921 Quality Care Products, LLC MIRTAZAPINE 15 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (83008-006-30)
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