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 141 条，共 8 页，当前第 5 页 ，可点击列名称排序
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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
63629-1840-2 63629-1840 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20081010 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63629-1840-2)
63629-1840-3 63629-1840 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20100304 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (63629-1840-3)
50090-0850-0 50090-0850 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA077584 A-S Medication Solutions PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-0850-0)
50090-0850-1 50090-0850 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA077584 A-S Medication Solutions PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-0850-1)
50090-0850-2 50090-0850 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA077584 A-S Medication Solutions PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-0850-2)
63629-1840-4 63629-1840 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20100323 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63629-1840-4)
68084-044-01 68084-044 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20050315 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)
68084-045-01 68084-045 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20050315 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)
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)
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)
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)
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)
65841-097-05 65841-097 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Lifesciences Limited PAROXETINE HYDROCHLORIDE ANHYDROUS 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65841-097-05)
65841-097-16 65841-097 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Lifesciences Limited PAROXETINE HYDROCHLORIDE ANHYDROUS 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65841-097-16)
65841-098-01 65841-098 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Lifesciences Limited PAROXETINE HYDROCHLORIDE ANHYDROUS 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65841-098-01)
65841-098-05 65841-098 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Lifesciences Limited PAROXETINE HYDROCHLORIDE ANHYDROUS 20 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65841-098-05)
65841-098-06 65841-098 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Lifesciences Limited PAROXETINE HYDROCHLORIDE ANHYDROUS 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65841-098-06)
65841-098-10 65841-098 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Lifesciences Limited PAROXETINE HYDROCHLORIDE ANHYDROUS 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65841-098-10)
65841-098-16 65841-098 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Lifesciences Limited PAROXETINE HYDROCHLORIDE ANHYDROUS 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65841-098-16)
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