Zileuton — ingredient monograph

Overview

Source: NDC Directory

Ingredient name

ZILEUTON

Base moiety

ZILEUTON

RxNorm CUI

730834

UNII

V1L22WVE2S

Medication products

5

Brand names

2

Dosage forms

5

FAERS reports

641 · not a risk measure

Products containing this ingredient

Source: NDC Directory 5 products

Zileuton Powder
8 NDC
Zileuton Tablet, Extended Release
Rx ANDA TE AB 1 NDC
ZYFLO zileuton · Tablet
Rx NDA 1 NDC
Zileuton Tablet, Film Coated, Extended Release
Rx ANDA TE AB 2 NDC
zileuton Tablet, Multilayer, Extended Release
Rx ANDA TE AB 2 NDC

Entries without a link are products listed by the FDA that carry no approval record, therapeutic equivalence rating or official labelling, so they have no detail page. Their facts are shown inline.

By dosage form

How this ingredient is presented across the catalogue.
Dosage form	Products	Examples
Powder	1	Zileuton
TABLET, Extended Release	1	Zileuton
Tablet	1	ZYFLO
TABLET, Film COATED, Extended Release	1	Zileuton
TABLET, MULTILAYER, Extended Release	1	zileuton

Sources for this page

Dataset	Agency	Used for
NDC Directory	FDA	Ingredient name, strengths, products, labelers, packages
DailyMed RxNorm mappings	NLM	RxNorm concept identifier (RxCUI)
FAERS	FDA	Adverse event report totals