NDC 71335-2348 – Prazosin hydrochloride

Prazosin Hydrochloride 5 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-2348

Product details

Brand name
Prazosin hydrochloride
Generic name
Prazosin hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA215697
Marketed since
January 3, 2023
Listing expires
December 31, 2026
Pharmacologic class
alpha-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Prazosin Hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
71335-2348-160 CAPSULE in 1 BOTTLE (71335-2348-1)Feb 21, 2024
71335-2348-230 CAPSULE in 1 BOTTLE (71335-2348-2)Feb 21, 2024

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