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=ANDA072192"
符合检索条件的记录共 3 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
69584-884-10 69584-884 HUMAN PRESCRIPTION DRUG Trazodone Hydrochloride Trazodone Hydrochloride TABLET, FILM COATED ORAL 20230101 N/A ANDA ANDA072192 Oxford Pharmaceuticals, LLC TRAZODONE HYDROCHLORIDE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69584-884-10)
69584-884-50 69584-884 HUMAN PRESCRIPTION DRUG Trazodone Hydrochloride Trazodone Hydrochloride TABLET, FILM COATED ORAL 20230101 N/A ANDA ANDA072192 Oxford Pharmaceuticals, LLC TRAZODONE HYDROCHLORIDE 50 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69584-884-50)
69584-884-90 69584-884 HUMAN PRESCRIPTION DRUG Trazodone Hydrochloride Trazodone Hydrochloride TABLET, FILM COATED ORAL 20230101 N/A ANDA ANDA072192 Oxford Pharmaceuticals, LLC TRAZODONE HYDROCHLORIDE 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69584-884-90)
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