Naproxen Tablet, Delayed Release
Product Images NDC 11534-211

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 11534-211). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sunrise Pharmaceutical, 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.

FDA Label Image

Chemical Structure (Naproxen 01)

FDA Label Image

Principal Display Panel (375 mg Tablet Bottle Label)

Principal Display Panel (375 mg Tablet Bottle Label)
This is a product label for Naproxen tablets containing 375 mg of naproxen. The tablets are delayed-release and come in a package of 100 tablets. The package is child-resistant and should be stored in light-resistant containers at 20° to 25°C (68° to 77°F). The medication guide should be dispensed to each patient by the pharmacist. The tablets are distributed by Sunrise Pharmaceutical, Inc. in Rahway, NJ.*
FDA Label Image

Principal Display Panel (500 mg Tablet Bottle Label)

Principal Display Panel (500 mg Tablet Bottle Label)
This is information about a medication with the NDC number 11534-212-01, Naproxen. Each tablet contains 500 mg of naproxen in delayed-release form. The packaging includes 100 tablets. The usual dosage instructions can be found in the package insert. The medication should be stored at 20°C to 25°C. It is recommended to dispense in light-resistant containers. This medication is distributed by Sunrise Pharmaceutical, located in Rahway, NJ 07065. The revision date is 09/25. *

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.