Ibuprofen Tablet, Film Coated
Product Images NDC 70010-068

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ibuprofen (NDC 70010-068). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Granules 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

Ibu-figure-01 (Ibu Figure 01)

Chemical structure of ibuprofen showing a benzene ring with attached isobutyl and carboxyl groups as part of the molecular arrangement.*

FDA Label Image

Ibu-400mg-30s (Ibu 400mg 30s)

Label of Ibuprofen Tablets, USP 400 mg film-coated tablets by Granules Pharmaceuticals Inc. The package contains 30 tablets. The label includes storage instructions and manufacturer details, stating the product is manufactured by Granules India Limited and distributed by Granules Pharmaceuticals Inc.*

FDA Label Image

Ibu-600mg-30s (Ibu 600mg 30s)

Label for Ibuprofen Tablets, USP 600 mg film-coated tablets. The packaging contains 30 tablets. It is manufactured by Granules India Limited, Hyderabad, India, and distributed by Granules Pharmaceuticals Inc., Chantilly, VA. The label includes storage instructions, dosage reference to package insert, and a barcode.*

FDA Label Image

Ibu-800mg-30s (Ibu 800mg 30s)

Label for Ibuprofen Tablets USP 800 mg film-coated tablets, containing 30 tablets per container. The label indicates it is Rx only, manufactured by Granules India Limited in Hyderabad, India and labeled for Granules Pharmaceuticals Inc., Chantilly, VA. Storage instructions and a URL for medication guides are included, along with a barcode and batch coding area.*

* 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.