Ibuprofen Tablet, Film Coated
Product Images NDC 43063-914

2 FDA label images from Pd-rx Pharmaceuticals, Inc. · 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 43063-914). 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

43063914 Label (43063914)

43063914 Label (43063914)
Label for Ibuprofen USP 800 mg film-coated tablets, containing 30 tablets per container. The label shows the brand Patient First, and indicates the product is Rx only. It advises dispensing in a tight/light resistant container and highlights the warning to keep out of children's reach. The label is by PD-Rx Pharmaceuticals, Inc., Oklahoma City, OK, with manufacturing by Marksans Pharma Ltd., India.*
FDA Label Image

Medguide Ibuprofen Tablets (Medication Guide For Nonsteroidal Anti Inflammatory Drugs)

Medguide Ibuprofen Tablets (Medication Guide For Nonsteroidal Anti Inflammatory Drugs)
This image shows a Medication Guide for Nonsteroidal Anti-Inflammatory Drugs (NSAIDs) detailing important safety information about NSAIDs such as increased risks of heart attack, stroke, bleeding, ulcers, and other side effects. It includes warnings on who should not take NSAIDs, potential side effects, drug interactions, and guidance on proper use. The guide also provides emergency symptoms requiring immediate medical attention and notes on aspirin and over-the-counter NSAID use. Manufacturer details are listed at the bottom.*

* 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.