Montelukast Tablet
Product Images NDC 68071-4034

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Montelukast (NDC 68071-4034). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare Pharmaceuticals,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

68071 4034 09

Product Information: Brand: Care Pharmaceuticals, Inc. Product name: Montelukast Sodium 10mg Tablets Size: #90 Tablets Lot Number: 000000 Manufacturer: Not specified National Drug Code (NDC): 68071-4034-09 Ingredients: Not available Expiry Date: 00-00 Description: The product is a pack of #90 tablets with a strength of Montelukast Sodium 10mg. The product is manufactured by Care Pharmaceuticals, Inc. The lot number of the product is 000000, and its expiry date is 00-00. The National Drug Code (NDC) of this product is 68071-4034-09. The product is meant for oral use only. Please consult your physician for any medical advice related to this medicine. Warning: The product should be kept out of reach of children and stored at a controlled temperature range of 59-86°F. In case of any side effects, contact your physician or report it to FDA.*

FDA Label Image

Montelukast-fig-1 (Montelukast Fig 1)

This data shows the mean percent change from baseline in a treatment study that lasted for 15 weeks. The study had a washout period and two treatment groups—one receiving a placebo and one receiving Montelukast Sodium.*

FDA Label Image

Montelukast-structural (Montelukast Structural)

* 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.