NDC 65862-249 – Alfuzosin Hydrochloride

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

Human Prescription Drug

Product NDC65862-249

Product details

Brand name
Alfuzosin Hydrochloride
Generic name
Alfuzosin Hydrochloride
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA079060
Marketed since
August 30, 2012
Listing expires
December 31, 2027
Pharmacologic class
alpha-Adrenergic Blocker

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
65862-249-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-01)Aug 30, 2012
65862-249-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-05)Aug 30, 2012
65862-249-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-30)Aug 30, 2012
65862-249-9090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-90)Aug 30, 2012
65862-249-991000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-99)Aug 30, 2012

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