Aurobindo Receives FDA Approval for Prazosin Hydrochloride Capsules USP, 1mg, 2mg and 5mg.
Published: April 03, 2023
Published: April 03, 2023
East Windsor, N.J. – Aurobindo Pharma Limited has received final approval from U.S. Food and Drug Administration for its Abbreviated New Drug Application Prazosin Hydrochloride Capsules USP, 1mg, 2mg and 5mg. Aurobindo Pharma’s Prazosin Hydrochloride Capsules, are an AB-rated generic equivalent to the reference listed drug (RLD), Minipress® Capsules manufactured by Pfizer Inc.
Prazosin Hydrochloride Capsules are indicated for: