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Last Updated: December 12, 2025

Details for New Drug Application (NDA): 207139

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NDA 207139 describes PAROXETINE MESYLATE, which is a drug marketed by Actavis Labs Fl Inc and Prinston Inc and is included in two NDAs. It is available from one supplier. Additional details are available on the PAROXETINE MESYLATE profile page.

The generic ingredient in PAROXETINE MESYLATE is paroxetine mesylate. There are thirty drug master file entries for this compound. Three suppliers are listed for this compound. Additional details are available on the paroxetine mesylate profile page.

Summary for 207139

Tradename:	PAROXETINE MESYLATE
Applicant:	Actavis Labs Fl Inc
Ingredient:	paroxetine mesylate
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	CAPSULE;ORAL			Strength	EQ 7.5MG BASE
Approval Date:	Jun 20, 2017	TE:	AB	RLD:	No

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