Ibuprofen Tablet, Film Coated
Product Images NDC 72789-218

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ibuprofen (NDC 72789-218). 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.

FDA Label Image

72789218 Label (72789218)

72789218 Label (72789218)
This is a warning label for a container of Ibuprofen tablets. The container is designed to be tight/light resistant and is not to be accessed by children. The medication is in 800mg strength and consists of 30 film-coated tablets. The container is identified by a code: 72789-218-30. The medication is manufactured by PHARMACEUTICALS, based in Oklahoma City. The label provides usage instructions for the medication, including taking it with food or milk, avoiding alcohol and aspirin, and informing one's physician about known or planned pregnancy. The label also advises seeking medical advice for side effects and provides details on dosage and storage instructions. Further information on the medication is available on an outsert included with the package. The label includes an expiry date: 12/2023, as well as other identification codes: GTIN:00372789218304 and LOT:L21C09, which may be useful in case of recalls or other issues.*
FDA Label Image

Chem Structure (C3f2b181 D310 4a4b Bb46 172c49d4b7e3 01)

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