Bupropion Hydrochloride Tablet, Film Coated, Extended Release
Product Images NDC 59651-511

View Photos of 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 Bupropion Hydrochloride (NDC 59651-511). 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 (150 mg (30 Tablets Bottle))

Package Label-principal Display Panel (150 mg (30 Tablets Bottle))
Label for Bupropion Hydrochloride Extended-Release Tablets, USP (XL) 150 mg by Aurobindo Pharma Limited. The label states the dosage form as film-coated extended-release tablets and a package size of 30 tablets. It includes usage instructions, storage conditions, distributor information, and a warning against combining with products containing bupropion hydrochloride.*
FDA Label Image

Package Label-principal Display Panel (300 mg (30 Tablets Bottle))

Package Label-principal Display Panel (300 mg (30 Tablets Bottle))
Label for Bupropion Hydrochloride Extended-Release Tablets USP (XL) 300 mg, film-coated and intended for once-daily oral use. The label includes storage instructions, warnings against use with Zyban and related products, and medication dispensing guidance. Distributed by Aurobindo Pharma USA, Inc. and manufactured in India. The package contains 30 tablets.*
FDA Label Image

Str (Bupropion Str)

Str (Bupropion Str)
Chemical structure of Bupropion Hydrochloride showing the molecular arrangement including a chlorophenyl group, a keto group, and a tert-butylamino substituent with associated hydrochloride (HCl).*

* 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.