Bupropion Hydrochloride Tablet, Film Coated
Product Images NDC 59651-875

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Bupropion Hydrochloride (NDC 59651-875). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma 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

Package Label-principal Display Panel (75 mg (100 Tablets Bottle))

Label for Bupropion Hydrochloride Tablets USP 75 mg film-coated tablets. The label includes warnings against use with Zyban or other bupropion products, pharmacist dispensing instructions, storage conditions, and distributor information for Aurobindo Pharma USA, Inc. It shows an image of a round tablet marked "75" and indicates a package of 100 tablets. The label notes the product is made in India and provides a web link for medication guides.*

FDA Label Image

Package Label-principal Display Panel (100 mg (100 Tablets Bottle))

Label for Bupropion Hydrochloride Tablets, USP 100 mg, film-coated oral tablets. The label includes a pill image marked "100" and indicates 100 tablets in the container. It lists Aurobindo Pharma Limited as the labeler with distribution by Aurobindo Pharma USA, Inc. Storage, handling warnings, and medication guide instructions are also present. The label features NDC 59651-875-01 and a barcode.*

FDA Label Image

Chemical Structure (Bupropion Str)

Chemical structure of bupropion hydrochloride showing the molecular arrangement including a chlorophenyl ring, a ketone group, and a tert-butylamino group attached to the phenyl ring with an associated hydrochloride salt.*

* 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.