NDC 72162-1449 – Alfuzosin Hydrochloride

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

Human Prescription Drug

Product NDC72162-1449

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 (1)

Package NDCDescriptionSince
72162-1449-990 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1449-9)Jul 16, 2024

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