NDC 57237-114 – Alfuzosin Hydrochloride

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

Human Prescription Drug

Product NDC57237-114

Product details

Brand name
Alfuzosin Hydrochloride
Generic name
Alfuzosin Hydrochloride
Labeler
Rising Pharma Holdings, Inc.
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 (3)

Package NDCDescriptionSince
57237-114-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (57237-114-01)Aug 30, 2012
57237-114-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (57237-114-05)Aug 30, 2012
57237-114-9090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (57237-114-90)Aug 30, 2012

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