Imuran Tablet
Product Images NDC 54766-590

3 FDA label images from Sebela Pharmaceuticals Inc. · 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 Imuran (NDC 54766-590). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sebela 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

Ca59010001 Imuran

Ca59010001 Imuran
IMURAN (azathioprine) 50 mg tablet carton label for oral use, distributed by Sebela Pharmaceuticals Inc. The label indicates 100 tablets per package with instructions to keep out of reach of children and store in a dry place at 20° to 25°C. The packaging features the product name, strength, bar code, and a QR code area with placeholders for lot and expiration date.*
FDA Label Image

Package Label (Lb59010001)

Package Label (Lb59010001)
Label for IMURAN (azathioprine) tablets, 50 mg strength, containing 100 tablets. The label displays the product name, active ingredient, dosage form, tablet strength, NDC number 54766-590-10, and specifies Rx only. It includes distributor information for Sebela Pharmaceuticals Inc. and storage instructions. A barcode and spaces for lot and expiration date are also visible.*
FDA Label Image

Structural Formula (Imu01 0003 01)

Structural Formula (Imu01 0003 01)
Chemical structure of azathioprine, the active ingredient in IMURAN tablets. The diagram depicts the molecular arrangement including nitrogen, sulfur, carbon, and oxygen atoms in azathioprine's chemical formula.*

* 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.