Uloric Tablet
Product Images NDC 64764-918

3 FDA label images from Takeda Pharmaceuticals America, Inc. · 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 Uloric (NDC 64764-918). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Takeda Pharmaceuticals America, 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

Chemical Structure (Uloric 01)

Chemical Structure (Uloric 01)
Chemical structure of febuxostat, the active ingredient in ULORIC. The diagram shows the molecular formula with labeled rings and functional groups including a carboxylic acid, nitrile, and thiazole ring, consistent with febuxostat's known chemical composition.*
FDA Label Image

40mg30ctbottlelabel (Uloric 02)

40mg30ctbottlelabel (Uloric 02)
ULORIC 40 mg tablets packaging label. The label displays the product name ULORIC with the generic name febuxostat below it. It indicates an oral tablet dosage form with a strength of 40 mg per tablet, containing 30 tablets in the package. The labeler is Takeda Pharmaceuticals America, Inc. Additional text includes storage instructions, dosage guidance, and a barcode.*
FDA Label Image

80mg30ctbottlelabel.jpg (Uloric 03)

80mg30ctbottlelabel.jpg (Uloric 03)
Label for Uloric (febuxostat) tablets 80 mg by Takeda Pharmaceuticals America, Inc. The label indicates a 30 tablet package, includes storage instructions at 25°C (77°F), dosage caution to see package insert, and a warning not to accept if bottle seal is broken or missing. The label also shows the NDC 64764-677-30 and barcode.*

* 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.