Bupropion Hydrochloride Tablet, Extended Release
Product Images NDC 70010-785

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 70010-785). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Granules 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

Bupropion-150-30s-label-jpg (Bupropion 150 30s Label Jpg)

Bupropion-150-30s-label-jpg (Bupropion 150 30s Label Jpg)
Label for Bupropion hydrochloride Extended-Release Tablets USP (XL), 150 mg, by Granules Pharmaceuticals Inc. The label indicates 30 tablets per package and includes usage instructions, warnings, storage conditions, and a barcode. It highlights that the medication is for once-daily oral use and warns against combining with Zybam or other bupropion-containing drugs.*
FDA Label Image

Bupropion-300-30s-label-jpg (Bupropion 300 30s Label Jpg)

Bupropion-300-30s-label-jpg (Bupropion 300 30s Label Jpg)
Label for Bupropion hydrochloride extended-release tablets, USP (XL), 300 mg strength. The product is labeled for once-daily oral use and contains 30 tablets. It includes warnings about not using in combination with Zyban or other bupropion-containing medicines. Manufactured by Granules Pharmaceuticals Inc., Chantilly, VA. The label also features storage instructions and a barcode.*
FDA Label Image

Bupropion-structure.jpg (Bupropion Structure)

Bupropion-structure.jpg (Bupropion Structure)
Chemical structure of bupropion hydrochloride showing the chlorophenyl ring, ketone group, and tert-butyl amine moiety with hydrochloride (HCl) indicated.*

* 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.