Ibuprofen Tablet, Film Coated
Product Images NDC 80425-0154

View Photos of 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 Ibuprofen (NDC 80425-0154). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Pharmacy 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

Ibuprofen 600mg Tab Qty 30 Ndc 80425 0154

Ibuprofen 600mg Tab Qty 30 Ndc 80425 0154
Label for Ibuprofen 600 mg film-coated tablets in a quantity of 30, labeled by Advanced Rx Pharmacy of Tennessee, LLC. The label includes the NDC 80425-0154-01 and indicates the storage instruction to keep at room temperature between 20 to 25 degrees Celsius (68 to 77 degrees Fahrenheit).*
FDA Label Image

Ibuprofen 600mg Tab Qty 60 Ndc 80425 0154

Ibuprofen 600mg Tab Qty 60 Ndc 80425 0154
Label for Ibuprofen 600 mg film-coated tablets, bottle of 60, labeled by Advanced Rx Pharmacy of Tennessee, LLC. The label includes NDC 80425-0154-02, lot number, expiration date 2/28/2023, storage instructions, and a barcode.*
FDA Label Image

Ibuprofen 600mg Tab Qty 90 Ndc 80425 0154

Ibuprofen 600mg Tab Qty 90 Ndc 80425 0154
Label for Ibuprofen 600 mg film-coated tablets, package size 90, labeled by Advanced Rx Pharmacy of Tennessee, LLC. The label includes the National Drug Code (NDC) 80425-0154, lot number 90IBU6001221 with an expiration date of 08/31/2022, and storage instructions at room temperature 20° to 25°C (68° to 77°F).*
FDA Label Image

Structure

Structure
Chemical structure of ibuprofen showing its molecular arrangement with a benzene ring bonded to isobutyl and carboxyl groups.*

* 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.