Montelukast Tablet, Film Coated
Product Images NDC 70518-3133

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)

FDA Label Image

Figure2.jpg (Figure2)

FDA Label Image

Montelukast Sodium 10mg 70518 3133 01

Montelukast Sodium 10mg Tablet is a medication manufactured by Camber Pharma, Inc. It comes in a pack of 30 tablets, with an NDC number of 70518-3133-01 and a source NDC number of 31722-0726-10. The medication should be kept out of the reach of children and stored between 20-26°C (63-77°F), with a permissible range of 15-30°C (59-86°F). The package insert should be consulted before use, and the medication has been repackaged by RemedyRepack Inc. in Indiana. No information is available regarding the expiration date or lot number.*

FDA Label Image

Remedy_label (Remedy Label)

Montelukast Sodium is a tablet with a dosage strength of 10 mg. Each container contains 90 tablets with an NDC of 70518-3133-00, and the LOT # and Source NDC are also provided. It is manufactured by Camber Pharma, Inc in Piscataway, N.J 08854. The package includes a direction insert, and it is recommended to keep the medicine in a dry place at a temperature of 20-26°C (63-77°F) and 15-30°C (59-86°F) [See USP]. Repackaging is done by RemedyRepack Inc. It is essential to keep the medication out of children's reach.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.