Ibuprofen Tablet, Film Coated
Product Images NDC 71610-532

3 FDA label images from Aphena Pharma Solutions - Tennessee, Llc · 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 Ibuprofen (NDC 71610-532). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aphena Pharma Solutions - Tennessee, Llc, 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

Bottle Label 600 mg (71610 0532 60)

Bottle Label 600 mg (71610 0532 60)
The packaging label for Ibuprofen USP 600 mg film-coated tablets, oral route. It includes the NDC 71610-0532 and states the storage temperature range of 20-25 degrees Celsius. The labeler is Aphena Pharma Solutions - Tennessee, LLC located in Cookeville, TN. The manufacturer is Marksans Pharma Limited, Verna, India. The label indicates the product is RX only and instructs storage in a light-resistant container. Contains quantity information and lot and expiration details.*
FDA Label Image

Aphena Pharma Solutions (TN)

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 text panel for Nonsteroidal Anti-Inflammatory Drugs (NSAIDs). It includes safety warnings about serious side effects, conditions for use, who should not take NSAIDs, and possible side effects. The guide also covers instructions on when to seek emergency help and general information about NSAIDs. Manufacturer details are provided 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.