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Medicines · US (FDA)

FDA 2011

Alpha-adrenoreceptor antagonists

Alfuzosin Hydrochloride

Approved 18 Jul 2011OralTablet, extended release

The FDA lists this product in 9 strengths and forms.

Official labelAsk Osler about it

On this page

Composition
Strengths and forms
Official product information

The table holds no label text for this product yet, only the facts beside it. The official product information has the full text.

Composition

Active ingredients: ALFUZOSIN HYDROCHLORIDE 10MG

Strengths and forms

The FDA lists each strength of a product separately; these pages share one label.

ALFUZOSIN HYDROCHLORIDE 10MG · Tablet, extended releaseANDA079013-001 · Prescription
ALFUZOSIN HYDROCHLORIDE 10MG · Tablet, extended releaseANDA079057-001 · Discontinued
ALFUZOSIN HYDROCHLORIDE 10MG · Tablet, extended releaseThis page
ALFUZOSIN HYDROCHLORIDE 10MG · Tablet, extended releaseANDA203192-001 · Prescription
ALFUZOSIN HYDROCHLORIDE 10MG · Tablet, extended releaseANDA079056-001 · Discontinued
ALFUZOSIN HYDROCHLORIDE 10MG · Tablet, extended releaseANDA079060-001 · Prescription
ALFUZOSIN HYDROCHLORIDE 10MG · Tablet, extended releaseANDA090221-001 · Discontinued
ALFUZOSIN HYDROCHLORIDE 10MG · Tablet, extended releaseANDA090284-001 · Prescription
ALFUZOSIN HYDROCHLORIDE 10MG · Tablet, extended releaseANDA079014-001 · Discontinued

Two medicines in one question?

Name two or more medicines and Osler runs an interaction check. A severe interaction is stated at the very top of the answer.

Official product information

Drugs@FDA lists the approved labels, letters and reviews for application ANDA079054.

Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.

At a glance

Brand name: Alfuzosin Hydrochloride
Drug class: Alpha-adrenoreceptor antagonists
Route: Oral
Dosage form: Tablet, extended release
Applicant: Torrent Pharms
Status: Discontinued
FDA approval: 18 Jul 2011
Application: ANDA079054-001
RxCUI: 46043