Bupropion Hydrochloride Tablet, Film Coated
Product Images NDC 0615-8582

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Bupropion Hydrochloride (NDC 0615-8582). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ncs Healthcare Of Ky, Llc Dba Vangard Labs, 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

Chemical Structure (Bupropion Tabs 8581 8582 1)

Chemical structure of bupropion hydrochloride, showing a chlorophenyl ring and functional groups including a ketone and a tertiary amine with three methyl groups, along with the hydrochloride salt (HCl).*

FDA Label Image

Principal Display Panel (Bupropion Tabs 8581 8582 2)

Bupropion Hydrochloride Tablets, USP 75 mg film-coated oral tablets labeled with NDC 0615-8581-39. The label includes lot number 8581 and quantity of 30 tablets. Manufactured by Aurobindo and packaged by Vangard Labs, Glasgow, KY 42141. Warning advises against use with Zyban or other bupropion hydrochloride products. Storage instructions indicate controlled room temperature and protection from light and moisture. Marked For Institutional Use Only.*

FDA Label Image

Principal Display Panel (Bupropion Tabs 8581 8582 3)

Label for Bupropion Hydrochloride Tablets, USP 100 mg, film-coated oral tablets, manufactured by Aurobindo and packaged by Vangard Labs. The label includes barcodes, lot number 8582, quantity of 30 tablets, storage instructions, warnings including not to use with Zyban or other bupropion hydrochloride-containing products, and institutional use only notice. The labeler is NCS HealthCare of KY, LLC dba Vangard Labs.*

* 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.