Montelukast Tablet, Film Coated
Product Images NDC 50090-6108

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Montelukast (NDC 50090-6108). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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

Figure1.jpg (Figure1)

Figure1.jpg (Figure1)
Chemical structure diagram of Montelukast, depicting its molecular components including aromatic rings, chlorine substitution, and other features characteristic of the active ingredient Montelukast.*
FDA Label Image

Figure2.jpg (Figure2)

Figure2.jpg (Figure2)
Line graph showing mean percent change from baseline over weeks of treatment comparing Montelukast Sodium and Placebo. The x-axis represents weeks of treatment up to 15 weeks, and the y-axis shows mean percent change. A washout period is indicated after week 12. Montelukast shows a higher increase compared to placebo throughout the treatment period.*
FDA Label Image

Camberlogo1 (Camberlogo1)

FDA Label Image

Camberlogo2 (Camberlogo2)

FDA Label Image

Label Image (Lbl500906108)

Label Image (Lbl500906108)
Montelukast 10 mg film coated tablets label from A-S Medication Solutions. The label specifies the active ingredient is montelukast sodium equivalent to 10 mg montelukast. It indicates storage instructions to keep between 68 to 77 degrees Fahrenheit, protected from moisture and light. Package contains 30 tablets.*

* 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.