Ibuprofen Tablet, Film Coated
Product Images NDC 68645-562

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ibuprofen (NDC 68645-562). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Legacy Pharmaceutical Packaging, 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

Ibuprofen-structure (Ibup 1)

FDA Label Image

Ibuprofen Tablets, Usp 600mg (Ibup 3)

Ibuprofen Tablets, Usp 600mg (Ibup 3)
IBUPROFEN Tablets, USP is a medication that comes in 600mg tablets. Each film-coated tablet contains Ibuprofen, USP 600 mg. This medication should be dispensed with a separate medication guide to each patient. The drug should be stored in a tight, light-resistant container as defined in USP and should be kept at 20° to 25°C (68° to 77°F) to avoid any excessive heat above 40°C (104°F). The usual dosage can be found on the package insert for dosage information. This medication is distributed by Granules India Limited and was made in India.*
FDA Label Image

Ibuprofen Tablets, Usp 800mg (Ibup 4)

Ibuprofen Tablets, Usp 800mg (Ibup 4)
IBUPROFEN Tablets is a USP drug used to treat pain, inflammation, and fever. Each film-coated tablet contains 800 mg of ibuprofen. The tablets come in a tightly sealed, light-resistant container and must be stored at room temperature. Granules India Limited has manufactured it, and it is being distributed by Wal-Mart in Bentonville, AR. The package contains 30 tablets, and each patient should be given a separate medication guide to follow the dosage instructions. No non-English characters were found.*

* 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.