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=ANDA078406"
符合检索条件的记录共 78 条，共 4 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
65862-155-05 65862-155 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 Aurobindo Pharma Limited PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-155-05)
65862-155-30 65862-155 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 Aurobindo Pharma Limited PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-155-30)
65862-155-90 65862-155 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 Aurobindo Pharma Limited PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65862-155-90)
65862-155-99 65862-155 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 Aurobindo Pharma Limited PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-155-99)
65862-156-05 65862-156 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 Aurobindo Pharma Limited PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-156-05)
65862-156-30 65862-156 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 Aurobindo Pharma Limited PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-156-30)
65862-156-90 65862-156 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 Aurobindo Pharma Limited PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65862-156-90)
65862-156-99 65862-156 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 Aurobindo Pharma Limited PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-156-99)
65862-156-01 65862-156 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 Aurobindo Pharma Limited PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-156-01)
65862-157-01 65862-157 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 Aurobindo Pharma Limited PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-157-01)
65862-157-05 65862-157 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 Aurobindo Pharma Limited PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-157-05)
65862-157-30 65862-157 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 Aurobindo Pharma Limited PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-157-30)
65862-157-90 65862-157 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 Aurobindo Pharma Limited PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65862-157-90)
65862-157-99 65862-157 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 Aurobindo Pharma Limited PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-157-99)
71610-056-15 71610-056 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20180502 N/A ANDA ANDA078406 Aphena Pharma Solutions - Tennessee, LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71610-056-15)
71610-056-45 71610-056 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20180502 N/A ANDA ANDA078406 Aphena Pharma Solutions - Tennessee, LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 45 TABLET, FILM COATED in 1 BOTTLE (71610-056-45)
16714-181-01 16714-181 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 NorthStar Rx LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (16714-181-01)
16714-181-02 16714-181 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 NorthStar Rx LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (16714-181-02)
16714-181-03 16714-181 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 NorthStar Rx LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16714-181-03)
16714-181-04 16714-181 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 NorthStar Rx LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (16714-181-04)
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