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 69 条，共 4 页，当前第 2 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
16714-183-01 16714-183 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 NorthStar Rx LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (16714-183-01)
16714-183-02 16714-183 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 NorthStar Rx LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (16714-183-02)
16714-183-03 16714-183 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 NorthStar Rx LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (16714-183-03)
50268-642-15 50268-642 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20160311 N/A ANDA ANDA078406 AvPAK PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-642-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-642-11)
65862-154-01 65862-154 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 Aurobindo Pharma Limited PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-154-01)
65862-154-05 65862-154 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 Aurobindo Pharma Limited PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-154-05)
65862-154-30 65862-154 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 Aurobindo Pharma Limited PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-154-30)
43353-713-15 43353-713 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20110322 N/A ANDA ANDA078406 Aphena Pharma Solutions - Tennessee, LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (43353-713-15)
43353-713-45 43353-713 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20180502 N/A ANDA ANDA078406 Aphena Pharma Solutions - Tennessee, LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 45 TABLET, FILM COATED in 1 BOTTLE (43353-713-45)
16714-184-01 16714-184 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 NorthStar Rx LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (16714-184-01)
16714-184-02 16714-184 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 NorthStar Rx LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (16714-184-02)
16714-184-03 16714-184 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 NorthStar Rx LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16714-184-03)
16714-184-04 16714-184 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 NorthStar Rx LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (16714-184-04)
16714-184-05 16714-184 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070725 N/A ANDA ANDA078406 NorthStar Rx LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (16714-184-05)
50268-643-15 50268-643 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20160311 N/A ANDA ANDA078406 AvPAK PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-643-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-643-11)
65862-155-01 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/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-155-01)
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)
13107-154-01 13107-154 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (13107-154-01)
13107-154-05 13107-154 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (13107-154-05)
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