NDC 76282-302 – Alfuzosin hydrochloride

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

Human Prescription Drug

Product NDC76282-302

Product details

Brand name
Alfuzosin hydrochloride
Generic name
Alfuzosin hydrochloride
Labeler
Exelan Pharmaceuticals Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA090284
Marketed since
October 2, 2012
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
76282-302-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-302-01)Oct 2, 2012
76282-302-05500 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-302-05)Oct 2, 2012
76282-302-101000 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-302-10)Oct 2, 2012
76282-302-12120 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-302-12)Dec 1, 2022
76282-302-9090 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-302-90)Jan 1, 2019

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