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 143 条，共 8 页，当前第 6 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)
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)
63629-1840-5 63629-1840 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20230301 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (63629-1840-5)
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)
65841-097-06 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 30 TABLET, FILM COATED in 1 BOTTLE (65841-097-06)
65841-097-10 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 1000 TABLET, FILM COATED in 1 BOTTLE (65841-097-10)
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)
63187-105-30 63187-105 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20150202 N/A ANDA ANDA077584 Proficient Rx LP PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63187-105-30)
63187-105-60 63187-105 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20150202 N/A ANDA ANDA077584 Proficient Rx LP PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63187-105-60)
63187-105-90 63187-105 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20150202 N/A ANDA ANDA077584 Proficient Rx LP PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-105-90)
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)
68382-099-06 68382-099 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Pharmaceuticals USA Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68382-099-06)
68382-099-10 68382-099 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Pharmaceuticals USA Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (68382-099-10)
68382-099-16 68382-099 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Pharmaceuticals USA Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68382-099-16)
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