Celecoxib Capsule
Product Images NDC 80425-0096

4 FDA label images from Advanced Rx Of Tennessee, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Celecoxib (NDC 80425-0096). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Of Tennessee, Llc, 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 Cap Qty 30 Ndc 80425 0096

Celecoxib 200mg Cap Qty 30 Ndc 80425 0096
Celecoxib 200 mg oral capsules in a package labeled for 30 capsules, manufactured by Advanced Rx of Tennessee, LLC, Nashville, TN. The label includes the National Drug Code (NDC) 80425-0096, lot number, expiration date, and storage instructions to store at room temperature 20° to 25°C (68° to 77°F). The label also states the product is compared to Celecoxib.*
FDA Label Image

Celecoxib 200mg Cap Qty 60 Ndc 80425 0096

Celecoxib 200mg Cap Qty 60 Ndc 80425 0096
Celecoxib 200 mg capsules, packaged by Advanced Rx of Tennessee, LLC, Nashville, TN. The label displays the product NDC 80425-0096, lot number 60CEX200422, and an expiration date of 4/30/2022. Storage instructions indicate room temperature 20°–25°C (68°–77°F). The package contains 60 capsules.*
FDA Label Image

Celecoxib 200mg Cap Qty 90 Ndc 80425 0096

Celecoxib 200mg Cap Qty 90 Ndc 80425 0096
Celecoxib 200 mg capsule label from Advanced Rx of Tennessee, LLC, indicating a package of 90 capsules. The label includes NDC code 80425-0096 and references a comparison to CELECOXIB. Storage instructions specify room temperature between 20° to 25°C (68° to 77°F).*
FDA Label Image

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Chemical structure diagram of the active ingredient Celecoxib, showing its molecular framework including a sulfonamide group, trifluoromethyl group, and aromatic 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.