Naproxen Tablet, Delayed Release
Product Images NDC 59651-987

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 Naproxen (NDC 59651-987). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, 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

Package Label-principal Display Panel (275 mg (100 Tablet Bottle))

Package Label-principal Display Panel (275 mg (100 Tablet Bottle))
Label for Naproxen Delayed-Release Tablets, USP 375 mg, oral tablets in a 100-count package by Aurobindo Pharma Limited. The label includes storage instructions, tamper-evident warnings, distributor and manufacturer details, and a website for medication guides. The NDC number is 59651-986-01.*
FDA Label Image

Package Label-principal Display Panel (550 mg (100 Tablet Bottle))

Package Label-principal Display Panel (550 mg (100 Tablet Bottle))
Label for Naproxen Delayed-Release Tablets USP 500 mg, oral tablets in a package of 100 tablets. Label includes storage instructions, tamper-evident container notice, distributor Aurobindo Pharma USA, Inc., and manufacturer Aurovitas Pharma Taizhou Co., Ltd. Barcode and imprint area for GTIN, serial number, expiry date, and lot number also visible.*
FDA Label Image

Chemical Structure (Naproxen Str)

Chemical Structure (Naproxen Str)
Chemical structure of Naproxen showing its molecular formula C14H14O3 and molecular weight 230.26. The diagram displays the two fused benzene rings with methoxy and carboxylic acid substituents characteristic of Naproxen.*

* 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.