Febuxostat Tablet
Product Images NDC 0527-2248

5 FDA label images from Lannett Company, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Febuxostat (NDC 0527-2248). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lannett Company, 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 (Febuxostat 01)

Chemical Structure (Febuxostat 01)
Chemical structure diagram of febuxostat, the active ingredient in FEBUXOSTAT tablets. The diagram shows the molecular structure with labeled functional groups and bonds typical of febuxostat.*
FDA Label Image

Label-40mg (Febuxostat 02)

Label-40mg (Febuxostat 02)
Label for Febuxostat Tablets 40 mg in a 30 tablet bottle by Lannett Company, Inc. The label indicates each tablet contains 40 mg of febuxostat. Storage instructions note to keep at 25°C (77°F) with permitted excursions between 15° to 30°C. The label also advises pharmacists to dispense the accompanying medication guide. The product is manufactured by Sunshine Lake Pharma Co., Ltd., Guangdong Province, China.*
FDA Label Image

Label-80 mg (Febuxostat 03)

Label-80 mg (Febuxostat 03)
Label for Febuxostat 80 mg tablets by Lannett Company, Inc. The label states each tablet contains 80 mg of febuxostat and includes storage instructions at 25°C (77°F) with allowable excursions. Manufactured by Sunshine Lake Pharma Co., Ltd. in Guangdong Province, China. The package contains 30 tablets with NDC 0527-2248-32.*
FDA Label Image

Logo0001-01 (Logo0001 01)

FDA Label Image

Logo0001 02

* 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.