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Last Updated: December 21, 2024

Details for New Drug Application (NDA): 072921

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NDA 072921 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 twenty-seven 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. Twenty-nine suppliers are listed for this compound. Additional details are available on the prazosin hydrochloride profile page.

Summary for 072921

Tradename:	PRAZOSIN HYDROCHLORIDE
Applicant:	Purepac Pharm
Ingredient:	prazosin hydrochloride
Patents:	0

Medical Subject Heading (MeSH) Categories for 072921

Adrenergic alpha-1 Receptor Antagonists
Antihypertensive Agents

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	CAPSULE;ORAL			Strength	EQ 2MG BASE
Approval Date:	May 16, 1989	TE:		RLD:	No

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