Allopurinol Tablet
Product Images NDC 70771-1907

4 FDA label images from Zydus Lifesciences Limited · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Allopurinol (NDC 70771-1907). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Lifesciences Limited, 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, the active ingredient shown as a heterocyclic compound with nitrogen atoms arranged in a fused ring system containing a ketone group, consistent with its known molecular framework.*
FDA Label Image

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Chemical structure diagram illustrating the metabolic pathway of Allopurinol, showing its conversion to Oxipurinol, Hypoxanthine, Xanthine, and Uric Acid. The diagram displays molecular structures connected by arrows indicating transformations among these compounds.*
FDA Label Image

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Allopurinol Tablets USP 100 mg oral tablet packaging label showing round beige tablets with imprint '1' and '209'. The label states the quantity as 100 tablets, prescription only, and indicates storage instructions. Manufactured by Cadila Healthcare Ltd, Baddi, India, and labeled by Zydus Lifesciences Limited.*
FDA Label Image

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Allopurinol Tablets USP 300 mg oral tablets packaging label showing two round tablets imprinted "H 2" and "10". The label includes dosage strength, NDC 70771-1127-1, quantity of 100 tablets, prescription only status, and manufacturer Cadila Healthcare Ltd., India. Storage and usage instructions are partially visible.*

* 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.