Zileuton Tablet, Extended Release
Product Images NDC 64980-206

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Zileuton (NDC 64980-206). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rising Pharma Holdings, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Zileuton Chemical Structure

Zileuton Chemical Structure
Chemical structure of Zileuton, illustrating its molecular framework with rings and functional groups including a thiophene ring, methyl group, hydroxyl group, amide, and amino substituents.*
FDA Label Image

Zileuton Container Label

Zileuton Container Label
Zileuton Extended-Release Tablets 600 mg label by Rising Pharma Holdings, Inc. The oral tablet package contains 120 tablets with directions for 2 tablets BID. The label includes warnings to dispense with patient information, usage and storage instructions, and features the NDC 64980-206-12 barcode and batch information area. Label dimensions are 140 mm by 60 mm.*
FDA Label Image

Zileuton Figure1

Zileuton Figure1
A line graph illustrating the mean change from baseline in trough FEV1 over multiple double-blind study weeks for Zileuton Extended-Release Tablets compared to placebo. The graph includes data points with a legend distinguishing Zileuton ER Tablets (solid line) from placebo (dotted line), showing relative improvement over time, with subject numbers listed below each time point.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.