NDC 71335-2146 – Alfuzosin Hydrochloride

Alfuzosin Hydrochloride 10 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC71335-2146

Product details

Brand name
Alfuzosin Hydrochloride
Generic name
Alfuzosin Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA079057
Marketed since
November 22, 2011
Listing expires
December 31, 2026
Pharmacologic class
alpha-Adrenergic Blocker

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
71335-2146-130 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-1)Apr 3, 2024
71335-2146-260 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-2)Apr 3, 2024
71335-2146-390 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-3)Jan 30, 2023
71335-2146-4120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-4)Apr 3, 2024
71335-2146-5100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-5)Apr 3, 2024

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