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Serving leading biopharmaceutical companies globally:

Moodys
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Generated: January 23, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 077082

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NDA 077082 describes PAROXETINE HYDROCHLORIDE, which is a drug marketed by Apotex Inc, Kremers Urban Pharms, Lupin Ltd, Mylan, Apotex, Aurobindo Pharma, Jubilant Generics, Mylan Pharms Inc, Oxford Pharms, Roxane, Sun Pharm Inds Inc, Teva, Teva Pharms, Upsher-smith Labs, and Zydus Pharms Usa, and is included in seventeen NDAs. It is available from fifty-four suppliers. Additional details are available on the PAROXETINE HYDROCHLORIDE profile page.

The generic ingredient in PAROXETINE HYDROCHLORIDE is paroxetine hydrochloride. There are thirty drug master file entries for this compound. Fifty-seven suppliers are listed for this compound. Additional details are available on the paroxetine hydrochloride profile page.
Summary for 077082
Tradename:PAROXETINE HYDROCHLORIDE
Applicant:Teva Pharms
Ingredient:paroxetine hydrochloride
Patents:0
Therapeutic Class:Antidepressants
Anxiolytics
Formulation / Manufacturing:see details

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrengthEQ 10MG BASE
Approval Date:Jun 29, 2007TE:RLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrengthEQ 20MG BASE
Approval Date:Jun 29, 2007TE:RLD:No

Profile for product number 003

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrengthEQ 30MG BASE
Approval Date:Jun 29, 2007TE:RLD:No

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Serving leading biopharmaceutical companies globally:

Queensland Health
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McKesson
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Johnson and Johnson
Colorcon
Medtronic
Fish and Richardson
Deloitte

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