NDC 31722-044 – Zileuton

Zileuton 600 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC31722-044

Product details

Brand name
Zileuton
Generic name
Zileuton
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA215742
Marketed since
October 11, 2022
Listing expires
December 31, 2026
Pharmacologic class
5-Lipoxygenase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Zileuton →

Package NDC codes (1)

Package NDCDescriptionSince
31722-044-12120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-044-12)Oct 11, 2022

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