Allopurinol Tablet
Product Images NDC 29300-349

View Photos of 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 Allopurinol (NDC 29300-349). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Unichem Pharmaceuticals (usa), 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

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Chemical structure of Allopurinol, showing the molecular arrangement of its atoms in a heterocyclic ring with nitrogen and oxygen atoms visible.*
FDA Label Image

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An illustration showing the chemical pathways involving Allopurinol and Oxipurinol, including conversions to Hypoxanthine, Xanthine, and Uric Acid. The diagram depicts molecular structures and chemical names, highlighting the metabolites related to Allopurinol metabolism.*
FDA Label Image

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FDA Label Image

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Allopurinol Tablets, USP 100 mg oral tablets label from Unichem Pharmaceuticals (USA), Inc. The label includes the NDC 29300-349-01, directions to store at 20° to 25°C in a light-resistant container, instructions to see package insert for indications and dosing, and a barcode. The product is prescription-only with a 100 tablet count. Manufacturer information for Unichem Laboratories Ltd. in India and Unichem Pharmaceuticals (USA) in New Jersey is also listed.*
FDA Label Image

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Allopurinol Tablets, USP 300 mg oral tablet packaging label from Unichem Pharmaceuticals (USA), Inc. The label indicates each scored tablet contains 300 mg of allopurinol and the package contains 100 tablets. Storage instructions specify keeping tablets at 20 to 25 degrees Celsius in a dry place. The label notes the drug is for prescription use only (Rx Only). Manufacturer details list Unichem Laboratories Ltd. in India and Unichem Pharmaceuticals (USA), Inc. in New Jersey.*

* 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.