Celecoxib
Product Images NDC 70518-3292

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Celecoxib (NDC 70518-3292). 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

Celecoxib 200mg 70518 3292 01

CELECOXIB 200 mg capsule package label showing a quantity of 30 capsules. The label includes the NDC 70518-3292-01 and is repackaged by RemedyRepack Inc. The label also notes manufacturing by Nivagen Pharmaceuticals, Inc., Sacramento, CA, and storage instructions at 20-25°C with permitted excursions. A QR code is displayed on the label as well.*

FDA Label Image

Celecoxib 200mg 70518 3292 02

Celecoxib 200 mg capsules packaging label showing a quantity of 60 capsules. The label includes the NDC number 70518-3292-02, manufacturer information for Nivagen Pharmaceuticals, Inc., and repackaging details by RemedyRepack Inc. The label advises to keep medication out of the reach of children and refers to the package insert for directions for use.*

FDA Label Image

Remedy_label (Remedy Label)

CELECOXIB 200 mg capsules packaging label shows a quantity of 90 capsules. The label includes the NDC number 70518-3292-00 and indicates the medication is repackaged by RemedyRepack Inc. Directions refer to the package insert, with storage temperature guidelines provided. Manufacturer is Nivagen Pharmaceuticals, Inc.*

FDA Label Image

Celecoxib-structure (Celecoxib Structure)

Chemical structure of celecoxib showing its molecular arrangement including sulfonamide and trifluoromethyl groups attached to a substituted pyrazole and benzene rings.*

* 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.