Celecoxib Capsule
Product Images NDC 0904-7550

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 0904-7550). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Major Pharmaceuticals, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

200mg Carton Label (3a1eadd5 C0a7 473e Bde0 6b9450d11c95 00)

200mg Carton Label (3a1eadd5 C0a7 473e Bde0 6b9450d11c95 00)
Unit dose blister pack label for Celecoxib 200 mg capsules by Major Pharmaceuticals. The label includes the NDC 0904-7551-61, dispensing instructions, quantity of 100 capsules (10 x 10), storage conditions, and a barcode. It notes Rx only and provides packaging and distribution information from Indianapolis, IN.*
FDA Label Image

100mg Carton Label (3a1eadd5 C0a7 473e Bde0 6b9450d11c95 01)

100mg Carton Label (3a1eadd5 C0a7 473e Bde0 6b9450d11c95 01)
Celecoxib 100 mg capsules unit dose packaging label from Major Pharmaceuticals. The label indicates a package of 100 capsules (10 x 10) for oral use. It includes storage instructions, dosage information referencing a product insert, and warnings about child safety and institutional use only. Labeler contact details and barcode are also visible.*
FDA Label Image

Structure (Celecoxib Structure)

Structure (Celecoxib Structure)
Chemical structure of celecoxib showing its molecular components with labeled bonds and aromatic rings, including the sulfonamide group, trifluoromethyl group, and methyl-substituted phenyl ring.*

* 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.