Montelukast Sodium Tablet, Film Coated
Product Images NDC 16729-119

3 FDA label images from Accord Healthcare Inc. · 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 16729-119). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Accord Healthcare 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.

FDA Label Image

Principal Display Panel (Montelukast 10mg 30)

Principal Display Panel (Montelukast 10mg 30)
Label for Montelukast Sodium Tablets USP, 10 mg oral film-coated tablets, packaged in a bottle of 30 tablets. The label indicates prescription use for adults 15 years and older, with storage instructions and manufacturer information for Accord Healthcare Inc. and Intas Pharmaceuticals Limited, India.*
FDA Label Image

Image Of Figure 1 (Montelukast Fig1)

Image Of Figure 1 (Montelukast Fig1)
A line graph comparing mean percent change from baseline over weeks in treatment between Montelukast Sodium Tablets (montelukast) and placebo groups. The horizontal axis shows weeks in treatment up to 15 weeks including a washout period; the vertical axis represents mean percent change from baseline. Montelukast Sodium group shows a sharper and higher increase compared to placebo, with a decline after washout begins.*
FDA Label Image

Image Of Chemical Structure (Montelukast Str)

Image Of Chemical Structure (Montelukast Str)
Chemical structure of Montelukast Sodium, showing its molecular framework including a chlorinated aromatic ring, a pyridine ring, and a sodium carboxylate group.*

* 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.