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
68382-001-01 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)
68382-001-16 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 90 TABLET, FILM COATED in 1 BOTTLE (68382-001-16)
68788-0797-1 68788-0797 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Preferred Pharmaceuticals, Inc PAROXETINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-0797-1)
68788-0797-3 68788-0797 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Preferred Pharmaceuticals, Inc PAROXETINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-0797-3)
68788-0797-6 68788-0797 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Preferred Pharmaceuticals, Inc PAROXETINE HYDROCHLORIDE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-0797-6)
68788-0797-8 68788-0797 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Preferred Pharmaceuticals, Inc PAROXETINE HYDROCHLORIDE 10 mg/1 120 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-0797-8)
68788-0797-9 68788-0797 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Preferred Pharmaceuticals, Inc PAROXETINE HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-0797-9)
71335-0321-1 71335-0321 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20180212 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0321-1)
71335-0321-2 71335-0321 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20211227 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-0321-2)
71335-0321-3 71335-0321 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20180517 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-0321-3)
71335-0321-4 71335-0321 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20211227 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71335-0321-4)
70518-3518-0 70518-3518 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20220913 N/A ANDA ANDA077584 REMEDYREPACK INC. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3518-0)
70518-3518-1 70518-3518 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20220929 N/A ANDA ANDA077584 REMEDYREPACK INC. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3518-1)
68788-6870-1 68788-6870 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20170111 N/A ANDA ANDA077584 Preferred Pharmaceuticals Inc. PAROXETINE HYDROCHLORIDE 40 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68788-6870-1)
68788-6870-3 68788-6870 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20170111 N/A ANDA ANDA077584 Preferred Pharmaceuticals Inc. PAROXETINE HYDROCHLORIDE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-6870-3)
68788-6870-6 68788-6870 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20170111 N/A ANDA ANDA077584 Preferred Pharmaceuticals Inc. PAROXETINE HYDROCHLORIDE 40 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-6870-6)
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)
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