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
68382-097-10 68382-097 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Pharmaceuticals USA Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (68382-097-10)
60760-398-90 60760-398 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20190320 N/A ANDA ANDA077584 St. Mary's Medical Park Pharmacy PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-398-90)
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)
68382-097-01 68382-097 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Pharmaceuticals USA Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68382-097-01)
68382-097-05 68382-097 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Pharmaceuticals USA Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (68382-097-05)
68382-099-16 68382-099 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20070413 N/A ANDA ANDA077584 Zydus Pharmaceuticals USA Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68382-099-16)
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)
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)
68788-9074-1 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)
68788-9074-3 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)
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)
63187-105-30 63187-105 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20150202 N/A ANDA ANDA077584 Proficient Rx LP PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63187-105-30)
63187-105-60 63187-105 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20150202 N/A ANDA ANDA077584 Proficient Rx LP PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63187-105-60)
63187-105-90 63187-105 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20150202 N/A ANDA ANDA077584 Proficient Rx LP PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-105-90)
63187-190-60 63187-190 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20150202 N/A ANDA ANDA077584 Proficient Rx LP PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63187-190-60)
63187-190-90 63187-190 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20150202 N/A ANDA ANDA077584 Proficient Rx LP PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-190-90)
63187-190-30 63187-190 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20150202 N/A ANDA ANDA077584 Proficient Rx LP PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63187-190-30)
50090-0850-1 50090-0850 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA077584 A-S Medication Solutions PAROXETINE HYDROCHLORIDE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-0850-1)
50090-0850-2 50090-0850 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA077584 A-S Medication Solutions PAROXETINE HYDROCHLORIDE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-0850-2)
61919-513-90 61919-513 HUMAN PRESCRIPTION DRUG PAROXETINE PAROXETINE TABLET, FILM COATED ORAL 20160229 N/A ANDA ANDA077584 DIRECT RX PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (61919-513-90)
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