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 142 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
68788-7410-8 68788-7410 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20180606 N/A ANDA ANDA077584 Preferred Pharmaceuticals Inc. PAROXETINE HYDROCHLORIDE 30 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (68788-7410-8)
68788-7410-9 68788-7410 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20180606 N/A ANDA ANDA077584 Preferred Pharmaceuticals Inc. PAROXETINE HYDROCHLORIDE 30 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-7410-9)
50090-0850-0 50090-0850 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA077584 A-S Medication Solutions PAROXETINE HYDROCHLORIDE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-0850-0)
50090-0850-1 50090-0850 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA077584 A-S Medication Solutions PAROXETINE HYDROCHLORIDE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-0850-1)
50090-0850-2 50090-0850 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA077584 A-S Medication Solutions PAROXETINE HYDROCHLORIDE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-0850-2)
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)
65841-098-01 65841-098 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Lifesciences Limited PAROXETINE HYDROCHLORIDE ANHYDROUS 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65841-098-01)
65841-098-05 65841-098 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Lifesciences Limited PAROXETINE HYDROCHLORIDE ANHYDROUS 20 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65841-098-05)
65841-098-06 65841-098 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Lifesciences Limited PAROXETINE HYDROCHLORIDE ANHYDROUS 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65841-098-06)
65841-098-10 65841-098 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Lifesciences Limited PAROXETINE HYDROCHLORIDE ANHYDROUS 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65841-098-10)
65841-098-16 65841-098 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Lifesciences Limited PAROXETINE HYDROCHLORIDE ANHYDROUS 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65841-098-16)
65841-099-01 65841-099 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Lifesciences Limited PAROXETINE HYDROCHLORIDE ANHYDROUS 30 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65841-099-01)
65841-099-05 65841-099 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Lifesciences Limited PAROXETINE HYDROCHLORIDE ANHYDROUS 30 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65841-099-05)
65841-099-06 65841-099 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Lifesciences Limited PAROXETINE HYDROCHLORIDE ANHYDROUS 30 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65841-099-06)
65841-099-10 65841-099 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Lifesciences Limited PAROXETINE HYDROCHLORIDE ANHYDROUS 30 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65841-099-10)
65841-099-16 65841-099 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Lifesciences Limited PAROXETINE HYDROCHLORIDE ANHYDROUS 30 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65841-099-16)
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