Montelukast Tablet, Film Coated
Product Images NDC 70518-3133

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Montelukast (NDC 70518-3133). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Figure1.jpg (Figure1)

Figure1.jpg (Figure1)
Chemical structure of montelukast, showing its molecular framework including aromatic rings, sulfur atom, and sodium carboxylate group as depicted in the image.*
FDA Label Image

Figure2.jpg (Figure2)

Figure2.jpg (Figure2)
A line graph showing mean percent change from baseline over weeks of treatment comparing Montelukast Sodium and placebo. The x-axis indicates weeks of treatment up to 15 weeks, including a washout period. Montelukast Sodium consistently shows higher mean percent change than placebo throughout the treatment and declines slightly during washout, while placebo remains low and stable.*
FDA Label Image

Montelukast Sodium 10mg 70518 3133 01

Montelukast Sodium 10mg 70518 3133 01
Montelukast Sodium 10 mg tablet label for a quantity of 30 tablets. The label shows the product name, strength, dosage form, and repackager RemedyRepack Inc. It includes storage instructions and a QR code, as well as manufacturer information stating MFG: Camber Pharma, Inc., Piscataway, NJ.*
FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Montelukast Sodium 10 mg tablet label showing a quantity of 90 tablets. The label includes the NDC number 70518-3133-00, manufacturer as Camber Pharma, Inc., Piscataway, NJ, and repackager RemedyRepack Inc., Indiana, PA. Directions note to see package insert and storage instructions at 20-25°C with permitted excursions. The label indicates RX only and advises keeping medication out of children's reach.*

* 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.