Naproxen Tablet, Delayed Release
Product Images NDC 72789-003

3 FDA label images from Pd-rx Pharmaceuticals, Inc. · 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 Naproxen (NDC 72789-003). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx Pharmaceuticals, Inc., 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

72789003 Label (72789003)

72789003 Label (72789003)
Label for Naproxen-DR USP 500 mg delayed-release tablets, containing 60 tablets per bottle. The label identifies PD-Rx Pharmaceuticals, Inc. of Oklahoma City, OK as the manufacturer. It includes warnings such as 'Rx only' and advises keeping the medication out of children's reach with dosage and storage instructions to see the package insert. The label states reorder number 110842, lot number H19D23, and expiration date 03/2021. Additional barcode and QR code are present, along with the NDC number 72789-003-60.*
FDA Label Image

Structural Formula (Naproxen Structure)

Structural Formula (Naproxen Structure)
Chemical structure of naproxen showing its molecular formula C14H14O3 and a molecular weight of 230.26.*
FDA Label Image

Structural Formula (Naproxen Table)

Structural Formula (Naproxen Table)
A data table comparing pharmacokinetic parameters between Naproxen Delayed-release Tablets 500 mg twice daily and Naproxen Tablets 500 mg twice daily. It presents values for Cmax (µg/mL), Tmax (hours), and AUC0-12 hr (µg·hr/mL) with mean values and coefficients of variation in parentheses.*

* 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.