Allopurinol Tablet
Product Images NDC 71205-208

View Photos of 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 Allopurinol (NDC 71205-208). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

Structure (Allopurinol 01)

Structure (Allopurinol 01)
Chemical structure of Allopurinol, showing a purine analog with characteristic ring structure and functional groups, consistent with the active ingredient Allopurinol.*
FDA Label Image

Figure (Allopurinol 02)

Figure (Allopurinol 02)
Chemical structure diagram illustrating the biochemical conversion relationships among Allopurinol, Oxipurinol, Hypoxanthine, Xanthine, and Uric Acid, showing their molecular forms and interconversions.*
FDA Label Image

71205-208-30 (Allopurinol 03)

71205-208-30 (Allopurinol 03)
Label for Allopurinol 100 mg tablets, packaged by Proficient Rx LP. The label indicates a count of 30 tablets per package, each containing 100 mg of Allopurinol USP. The tablets are described as round, white, scored, and debossed with 'MP 71.' Manufacturer information is provided for ALKALOIDA Chemical Company Zrt in Hungary. Storage instructions specify maintaining a temperature between 20° to 25°C (68° to 77°F). The label includes various codes such as NDC 71205-208-30 and GTIN 00371205208301, along with placeholders for lot number, serial number, and expiration date.*

* 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.