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Last Updated: December 13, 2025

Details for New Drug Application (NDA): 072609

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NDA 072609 describes PRAZOSIN HYDROCHLORIDE, which is a drug marketed by Alembic, Am Therap, Ani Pharms, Appco, Aurobindo Pharma Ltd, Dava Pharms Inc, Granules, Lannett Co Inc, Mankind Pharma, MSN, Mylan, Novitium Pharma, Purepac Pharm, Teva Pharms, and Watson Labs, and is included in twenty-three NDAs. It is available from thirty-one suppliers. Additional details are available on the PRAZOSIN HYDROCHLORIDE profile page.

The generic ingredient in PRAZOSIN HYDROCHLORIDE is prazosin hydrochloride. There are seventeen drug master file entries for this compound. Thirty-two suppliers are listed for this compound. Additional details are available on the prazosin hydrochloride profile page.

Summary for 072609

Tradename:	PRAZOSIN HYDROCHLORIDE
Applicant:	Watson Labs
Ingredient:	prazosin hydrochloride
Patents:	0

Medical Subject Heading (MeSH) Categories for 072609

Adrenergic alpha-1 Receptor Antagonists
Antihypertensive Agents

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	CAPSULE;ORAL			Strength	EQ 5MG BASE
Approval Date:	May 16, 1989	TE:		RLD:	No

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