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"
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
71335-0321-1 71335-0321 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20180212 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0321-1)
71335-0321-2 71335-0321 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20211227 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-0321-2)
71335-0321-3 71335-0321 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20180517 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-0321-3)
71335-0321-4 71335-0321 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20211227 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71335-0321-4)
55289-972-30 55289-972 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20160210 N/A ANDA ANDA077584 PD-Rx Pharmaceuticals, Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-972-30)
55289-972-60 55289-972 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20160210 N/A ANDA ANDA077584 PD-Rx Pharmaceuticals, Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-972-60)
55289-972-90 55289-972 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20160210 N/A ANDA ANDA077584 PD-Rx Pharmaceuticals, Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-972-90)
71335-0544-2 71335-0544 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20220209 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-0544-2)
71335-0544-5 71335-0544 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20220209 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71335-0544-5)
71335-0544-6 71335-0544 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20220209 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-0544-6)
71335-0544-7 71335-0544 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20220209 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71335-0544-7)
71335-0544-3 71335-0544 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20220209 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-0544-3)
71335-0544-4 71335-0544 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20220209 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-0544-4)
71335-0544-1 71335-0544 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20220209 N/A ANDA ANDA077584 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0544-1)
68788-9074-1 68788-9074 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Preferred Pharmaceuticals, Inc PAROXETINE HYDROCHLORIDE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9074-1)
68788-9074-9 68788-9074 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Preferred Pharmaceuticals, Inc PAROXETINE HYDROCHLORIDE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9074-9)
68788-9074-3 68788-9074 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Preferred Pharmaceuticals, Inc PAROXETINE HYDROCHLORIDE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9074-3)
60760-501-90 60760-501 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20190320 N/A ANDA ANDA077584 St. Mary's Medical Park Pharmacy PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-501-90)
68788-9074-6 68788-9074 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Preferred Pharmaceuticals, Inc PAROXETINE HYDROCHLORIDE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9074-6)
68788-9074-8 68788-9074 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine Hydrochloride TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Preferred Pharmaceuticals, Inc PAROXETINE HYDROCHLORIDE 20 mg/1 120 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9074-8)
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