Allopurinol Tablet
Product Images NDC 0378-0137

View Photos of 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 0378-0137). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan Pharmaceuticals 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

Image 01

Image 01
Chemical structure of allopurinol, depicting its bicyclic ring system with nitrogen atoms and an oxygen double bond.*
FDA Label Image

Image 02

Image 02
Chemical structure diagram illustrating the metabolic pathway of allopurinol, showing conversions between allopurinol, oxipurinol, hypoxanthine, xanthine, and uric acid with their respective molecular structures and names.*
FDA Label Image

Image 03

Image 03
Label for Allopurinol 100 mg oral tablets by Mylan Pharmaceuticals Inc. The label states the active ingredient as allopurinol USP. It specifies the quantity as 100 tablets, includes the National Drug Code (NDC) 0378-0137-01, and contains storage and handling instructions, emphasizing child-resistant packaging and temperature control.*
FDA Label Image

Image 04

Image 04
Allopurinol 300 mg oral tablets label from Mylan Pharmaceuticals Inc. The label shows the product name, strength, and dosage form, specifying 100 tablets per container. It includes instructions for dispensing, storage conditions at controlled room temperature, and manufacturer details. The label also features a barcode, tablet imprint M 71, and safety warnings regarding child resistance and medication handling.*

* 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.