Celecoxib Capsule
Product Images NDC 67296-2236

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Celecoxib (NDC 67296-2236). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Chemical Structure (Celecoxib 01)

Chemical Structure (Celecoxib 01)
Chemical structure of the active ingredient Celecoxib, showing the molecular arrangement with labeled functional groups including sulfonamide, trifluoromethyl, and methyl substituents on aromatic rings.*
FDA Label Image

Principal Display Panel (100 mg Capsule Bottle Label)

Principal Display Panel (100 mg Capsule Bottle Label)
Label for Celecoxib Capsules, 100 mg strength, oral capsule dosage form. The label indicates the product contains 500 capsules and is for prescription use only. It is manufactured by CSPC OuYI Pharmaceutical Co., Ltd and labeled for Westminster Pharmaceuticals, LLC. Storage and dispensing instructions are included along with a pharmacist notice to dispense the medication guide.*
FDA Label Image

Principal Display Panel (200 mg Capsule Bottle Label)

Principal Display Panel (200 mg Capsule Bottle Label)
Label for Celecoxib Capsules 200 mg showing a package size of 500 capsules. The label includes directions for prescription use (Rx Only), storage instructions, and manufacturer information, noting CSPC Ouiyi Pharmaceutical Co., Ltd., and Westminster Pharmaceuticals. The label displays the NDC 69367-302-05 and features the Westminster Pharmaceuticals logo.*

* 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.