NDC 47335-956 – Alfuzosin Hydrochloride

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

Human Prescription Drug 1 recall

Product NDC47335-956

Product details

Brand name
Alfuzosin Hydrochloride
Generic name
Alfuzosin Hydrochloride
Labeler
Sun Pharmaceutical Industries, Inc.
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
47335-956-08100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-08)Nov 22, 2011
47335-956-181000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-18)Nov 22, 2011
47335-956-8190 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-81)Nov 22, 2011
47335-956-8330 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-83)Nov 22, 2011
47335-956-88100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-88)Nov 22, 2011

Recalls mentioning this NDC

Other Alfuzosin Hydrochloride products