NDC 71335-2311 – Prazosin hydrochloride

Prazosin Hydrochloride 2 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-2311

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 (5)

Package NDCDescriptionSince
71335-2311-130 CAPSULE in 1 BOTTLE (71335-2311-1)Dec 21, 2023
71335-2311-228 CAPSULE in 1 BOTTLE (71335-2311-2)Dec 21, 2023
71335-2311-360 CAPSULE in 1 BOTTLE (71335-2311-3)Dec 21, 2023
71335-2311-490 CAPSULE in 1 BOTTLE (71335-2311-4)Dec 21, 2023
71335-2311-518 CAPSULE in 1 BOTTLE (71335-2311-5)Dec 21, 2023

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