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
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)
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)
50268-640-15 50268-640 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20160311 N/A ANDA ANDA078406 AvPAK PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-640-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-640-11)
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)
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)
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)
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)
13107-154-30 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 30 TABLET, FILM COATED in 1 BOTTLE (13107-154-30)
13107-154-90 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 90 TABLET, FILM COATED in 1 BOTTLE (13107-154-90)
13107-154-99 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 1000 TABLET, FILM COATED in 1 BOTTLE (13107-154-99)
13107-155-01 13107-155 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (13107-155-01)
13107-155-05 13107-155 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (13107-155-05)
13107-155-30 13107-155 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (13107-155-30)
13107-155-90 13107-155 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (13107-155-90)
13107-155-99 13107-155 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (13107-155-99)
13107-156-01 13107-156 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (13107-156-01)
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