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 145 条，共 8 页，当前第 4 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
65841-601-06 65841-601 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Lifesciences Limited PAROXETINE HYDROCHLORIDE ANHYDROUS 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65841-601-06)
65841-601-10 65841-601 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Lifesciences Limited PAROXETINE HYDROCHLORIDE ANHYDROUS 40 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65841-601-10)
65841-601-16 65841-601 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Lifesciences Limited PAROXETINE HYDROCHLORIDE ANHYDROUS 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65841-601-16)
71335-0544-2 71335-0544 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20220209 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-0544-2)
71335-0544-3 71335-0544 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20220209 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-0544-3)
71335-0544-4 71335-0544 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20220209 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-0544-4)
71335-0544-5 71335-0544 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20220209 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71335-0544-5)
71335-0544-6 71335-0544 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20220209 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-0544-6)
71335-0544-7 71335-0544 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20220209 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71335-0544-7)
68382-001-01 68382-001 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Pharmaceuticals USA Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68382-001-01)
68382-001-05 68382-001 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Pharmaceuticals USA Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (68382-001-05)
68382-001-06 68382-001 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Pharmaceuticals USA Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68382-001-06)
68382-001-10 68382-001 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Pharmaceuticals USA Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (68382-001-10)
68788-6870-8 68788-6870 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20170111 N/A ANDA ANDA077584 Preferred Pharmaceuticals Inc. PAROXETINE HYDROCHLORIDE 40 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (68788-6870-8)
68788-6870-9 68788-6870 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20170111 N/A ANDA ANDA077584 Preferred Pharmaceuticals Inc. PAROXETINE HYDROCHLORIDE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-6870-9)
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)
76420-718-01 76420-718 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA077584 Asclemed USA, Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-718-01)
76420-718-05 76420-718 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA077584 Asclemed USA, Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76420-718-05)
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