Allopurinol Tablet
Product Images NDC 16729-135

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Allopurinol (NDC 16729-135). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Accord Healthcare 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

Figure (Allopurinol Fig 1)

An illustration showing the chemical structures and interconversion pathways of Allopurinol, Oxipurinol, Hypoxanthine, Xanthine, and Uric Acid with their chemical names and formulas. Arrows indicate the metabolic or chemical relationships between these purine-related compounds.*

FDA Label Image

Structural Formula (Allopurinol Structure)

Chemical structure of Allopurinol showing a fused bicyclic ring system with nitrogen atoms and an oxygen double bond, representing the molecular arrangement of the active ingredient Allopurinol.*

FDA Label Image

100 mg 500 Tablets Bottle (Allopurinol Tablets 100 500)

Label for Allopurinol Tablets USP 100 mg by Accord Healthcare Inc., contains 500 oral tablets. Label includes storage instructions, manufacturing details by Intas Pharmaceuticals Limited, and NDC 16729-134-16. Features barcode and space for lot and expiration data.*

FDA Label Image

300 mg 500 Tablets Bottle (Allopurinol Tablets 300 500)

Label for Allopurinol Tablets USP 300 mg oral tablets by Accord Healthcare Inc. The label shows the NDC number 16729-135-16 and indicates a package size of 500 tablets. Storage instructions specify 20° to 25°C and dispensing in a tight, light-resistant container. Manufactured by Intas Pharmaceuticals Limited, India. The label includes barcodes and space for overcoding lot and expiration data.*

* 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.