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=ANDA077584"
符合检索条件的记录共 149 条，共 8 页，当前第 6 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
50090-1297-1 50090-1297 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA077584 A-S Medication Solutions PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-1297-1)
50090-1297-0 50090-1297 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA077584 A-S Medication Solutions PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-1297-0)
55289-972-90 55289-972 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20160210 N/A ANDA ANDA077584 PD-Rx Pharmaceuticals, Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-972-90)
55289-972-30 55289-972 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20160210 N/A ANDA ANDA077584 PD-Rx Pharmaceuticals, Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-972-30)
55289-972-60 55289-972 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20160210 N/A ANDA ANDA077584 PD-Rx Pharmaceuticals, Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-972-60)
60760-501-90 60760-501 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20190320 N/A ANDA ANDA077584 St. Mary's Medical Park Pharmacy PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-501-90)
60760-398-90 60760-398 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20190320 N/A ANDA ANDA077584 St. Mary's Medical Park Pharmacy PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-398-90)
68071-1740-1 68071-1740 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20170818 N/A ANDA ANDA077584 NuCare Pharmaceuticals,Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-1740-1)
63629-3349-3 63629-3349 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20100317 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63629-3349-3)
63629-3349-1 63629-3349 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20090904 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63629-3349-1)
63629-3349-2 63629-3349 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20100301 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63629-3349-2)
68084-045-01 68084-045 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20080318 N/A ANDA ANDA077584 American Health Packaging PAROXETINE HYDROCHLORIDE 20 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-045-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-045-11)
68084-046-01 68084-046 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20080110 N/A ANDA ANDA077584 American Health Packaging PAROXETINE HYDROCHLORIDE 30 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-046-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-046-11)
68084-047-01 68084-047 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20080618 N/A ANDA ANDA077584 American Health Packaging PAROXETINE HYDROCHLORIDE 40 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-047-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-047-11)
68084-044-01 68084-044 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20080116 N/A ANDA ANDA077584 American Health Packaging PAROXETINE HYDROCHLORIDE 10 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-044-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-044-11)
68788-9074-1 68788-9074 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Preferred Pharmaceuticals, Inc PAROXETINE HYDROCHLORIDE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9074-1)
68788-9074-9 68788-9074 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Preferred Pharmaceuticals, Inc PAROXETINE HYDROCHLORIDE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9074-9)
70518-0003-0 70518-0003 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20161123 N/A ANDA ANDA077584 REMEDYREPACK INC. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0003-0)
70518-0003-1 70518-0003 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20220601 N/A ANDA ANDA077584 REMEDYREPACK INC. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0003-1)
70518-0003-2 70518-0003 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20240501 N/A ANDA ANDA077584 REMEDYREPACK INC. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 30 POUCH in 1 BOX (70518-0003-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-0003-3)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase