Montelukast Sodium
Product Images NDC 53808-0920

3 FDA label images from State Of Florida Doh Central Pharmacy · 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 Montelukast Sodium (NDC 53808-0920). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by State Of Florida Doh Central Pharmacy, 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

Label Image For 10mg (10mg Greenstone)

Label Image For 10mg (10mg Greenstone)
Label for Montelukast Sodium 10 mg tablets from State of Florida DOH Central Pharmacy. The label shows a quantity of 30 tablets with prescription-only status. It includes lot number information, an expiration date of 01/23/2014, and a barcode with UPC 359762003027.*
FDA Label Image

Figure 1: Fev1 Mean Percent Change From Baseline (Montelukast Fig1)

Figure 1: Fev1 Mean Percent Change From Baseline (Montelukast Fig1)
A line graph showing the mean percent change from baseline in FEV1 over weeks of treatment and washout period in a U.S. trial comparing Montelukast Sodium (N=406) and placebo (N=270). The x-axis represents weeks in treatment and the y-axis represents mean percent change from baseline. Montelukast Sodium shows a higher increase in FEV1 over time compared to placebo, with a decline during washout.*
FDA Label Image

Chemical Structure (Montelukast Str)

Chemical Structure (Montelukast Str)
Chemical structure of Montelukast Sodium, showing its molecular framework including aromatic rings, sulfur atom, and sodium carboxylate group, consistent with the active ingredient Montelukast Sodium.*

* 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.