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Prazosin

Generic Name
Prazosin
Brand Names
Minipress, Minizide
Drug Type
Small Molecule
Chemical Formula
C19H21N5O4
CAS Number
19216-56-9
Unique Ingredient Identifier
XM03YJ541D

Overview

Prazosin is a drug used to treat hypertension. Prazosin is marketed by Pfizer and was initially approved by the FDA in 1988. It belongs to the class of drugs known as alpha-1 antagonists. Recently, many studies have evaluated the benefits of this drug in controlling the symptoms of post-traumatic stress disorder (PTSD) and associated nightmares.

Background

Prazosin is a drug used to treat hypertension. Prazosin is marketed by Pfizer and was initially approved by the FDA in 1988. It belongs to the class of drugs known as alpha-1 antagonists. Recently, many studies have evaluated the benefits of this drug in controlling the symptoms of post-traumatic stress disorder (PTSD) and associated nightmares.

Indication

This drug is indicated for the treatment of hypertension (high blood pressure). Prazosin can be given alone or given with other blood pressure-lowering drugs, including diuretics or beta-adrenergic blocking agents . Prazosin does not negatively impact lung function, and therefore may be used to manage hypertension in patients who are asthmatic or patients with chronic obstructive lung disease (COPD).

Associated Conditions

  • Agitation
  • Benign Prostatic Hyperplasia (BPH)
  • Hypertension
  • Raynaud's Phenomenon
  • Disturbed sleep/nightmares

FDA Approved Products

Prazosin HCL
Manufacturer:Direct_Rx
Route:ORAL
Strength:2 mg in 1 1
Approved: 2024/03/06
NDC:72189-540
Prazosin Hydrochloride
Manufacturer:Physicians Total Care, Inc.
Route:ORAL
Strength:2 mg in 1 1
Approved: 2012/09/19
NDC:54868-1547
Prazosin Hydrochloride
Manufacturer:Aurobindo Pharma Limited
Route:ORAL
Strength:2 mg in 1 1
Approved: 2023/02/16
NDC:59651-272
Prazosin Hydrochloride
Manufacturer:Marlex Pharmaceuticals Inc
Route:ORAL
Strength:5 mg in 1 1
Approved: 2023/11/17
NDC:10135-668
Prazosin Hydrochloride
Manufacturer:Aurobindo Pharma Limited
Route:ORAL
Strength:1 mg in 1 1
Approved: 2023/02/16
NDC:59651-271

Singapore Approved Products

No Singapore products found for this drug

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