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"
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
13107-157-30 13107-157 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (13107-157-30)
13107-157-90 13107-157 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (13107-157-90)
13107-157-99 13107-157 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (13107-157-99)
63187-564-30 63187-564 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20181201 N/A ANDA ANDA078406 Proficient Rx LP PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63187-564-30)
63187-564-60 63187-564 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20181201 N/A ANDA ANDA078406 Proficient Rx LP PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63187-564-60)
63187-564-90 63187-564 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20181201 N/A ANDA ANDA078406 Proficient Rx LP PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-564-90)
70518-3277-2 70518-3277 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20231207 N/A ANDA ANDA078406 REMEDYREPACK INC. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3277-2)
0615-8359-39 0615-8359 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20201111 N/A ANDA ANDA078406 NCS HealthCare of KY, LLC dba Vangard Labs PAROXETINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8359-39)
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)
43353-845-15 43353-845 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20170726 N/A ANDA ANDA078406 Aphena Pharma Solutions - Tennessee, LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (43353-845-15)
43353-845-45 43353-845 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20170808 N/A ANDA ANDA078406 Aphena Pharma Solutions - Tennessee, LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 45 TABLET, FILM COATED in 1 BOTTLE (43353-845-45)
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)
43353-994-15 43353-994 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20150205 N/A ANDA ANDA078406 Aphena Pharma Solutions - Tennessee, LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (43353-994-15)
43353-994-45 43353-994 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20150205 N/A ANDA ANDA078406 Aphena Pharma Solutions - Tennessee, LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 45 TABLET, FILM COATED in 1 BOTTLE (43353-994-45)
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)
65862-154-90 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 90 TABLET, FILM COATED in 1 BOTTLE (65862-154-90)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase