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"
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
68382-097-05 68382-097 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Pharmaceuticals USA Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (68382-097-05)
68382-097-06 68382-097 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Pharmaceuticals USA Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68382-097-06)
68382-097-10 68382-097 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Pharmaceuticals USA Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (68382-097-10)
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)
63629-3349-3 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)
68788-9074-3 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 30 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9074-3)
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)
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)
68788-9074-6 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 60 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9074-6)
68788-9074-8 68788-9074 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Preferred Pharmaceuticals, Inc PAROXETINE HYDROCHLORIDE 20 mg/1 120 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9074-8)
76420-716-10 76420-716 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA077584 Asclemed USA, Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (76420-716-10)
76420-716-30 76420-716 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA077584 Asclemed USA, Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-716-30)
76420-716-60 76420-716 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA077584 Asclemed USA, Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-716-60)
76420-717-01 76420-717 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA077584 Asclemed USA, Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-717-01)
76420-717-05 76420-717 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA077584 Asclemed USA, Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76420-717-05)
76420-717-10 76420-717 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA077584 Asclemed USA, Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (76420-717-10)
76420-717-30 76420-717 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA077584 Asclemed USA, Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-717-30)
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