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 3 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
68382-097-01 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/1 100 TABLET, FILM COATED in 1 BOTTLE (68382-097-01)
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)
68382-097-16 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 90 TABLET, FILM COATED in 1 BOTTLE (68382-097-16)
67046-1013-3 67046-1013 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20241108 N/A ANDA ANDA077584 Coupler LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1013-3)
80425-0339-1 80425-0339 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20230519 N/A ANDA ANDA077584 Advanced Rx Pharmacy of Tennessee, LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (80425-0339-1)
70518-3518-2 70518-3518 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20250131 N/A ANDA ANDA077584 REMEDYREPACK INC. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 100 POUCH in 1 BOX (70518-3518-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-3518-3)
70518-3518-4 70518-3518 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20250618 N/A ANDA ANDA077584 REMEDYREPACK INC. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3518-4)
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)
68788-9074-3 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)
68788-9074-6 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)
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)
68788-6870-1 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)
65841-097-01 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/1 100 TABLET, FILM COATED in 1 BOTTLE (65841-097-01)
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)
63187-434-30 63187-434 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20150202 N/A ANDA ANDA077584 Proficient Rx LP PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63187-434-30)
63187-434-60 63187-434 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20150202 N/A ANDA ANDA077584 Proficient Rx LP PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63187-434-60)
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