Celecoxib
Product Images NDC 63739-297

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 63739-297). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mckesson Corporation Dba Sky Packaging, 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

333 (Celecoxib Capsules 100 mg Non Cr Old)

333 (Celecoxib Capsules 100 mg Non Cr Old)
Packaging label for Celecoxib Capsules 100 mg by McKesson Corporation dba SKY Packaging. The label indicates a 100-capsule supply (10 x 10 unit dose) with instructions for use and storage, including pharmacist guidance to dispense the accompanying Medication Guide. Barcode and lot/expiration data placeholders are present.*
FDA Label Image

444 (Celecoxib Capsules 200 mg Non Cr Old)

444 (Celecoxib Capsules 200 mg Non Cr Old)
Celecoxib Capsules 200 mg package label shows a white carton with blue and black text. The label includes the product name, strength (200 mg), and dosage form (capsules). It states a quantity of 100 capsules (10 x 10 unit dose) and instructs pharmacists to dispense the accompanying medication guide. Labeler is McKesson Corporation dba SKY Packaging. Storage instructions and medication guide contact info are also visible, alongside barcode and opening instructions for the blister pack.*
FDA Label Image

Structure (Celecoxib Structure)

Structure (Celecoxib Structure)
Chemical structure of celecoxib showing its molecular framework including sulfonamide, trifluoromethyl, methyl, and pyrazole groups as connected in the diagram.*

* 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.