Bupropion Hydrochloride Tablet, Extended Release
Product Images NDC 50268-133

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 50268-133). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avpak, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

1 (133 13)

1 (133 13)
The label for Bupropion Hydrochloride extended-release tablets, USP (XL), 150 mg strength, manufactured by AvPAK. The label indicates a once-daily oral tablet dosage form, with packaging containing 30 tablets in unit dose format (6 blister cards by 5 tablets each). The label includes regulatory warnings, storage instructions, and a barcode. The AvPAK logo appears at the bottom of the label.*
FDA Label Image

1 (134 13)

1 (134 13)
Label for Bupropion Hydrochloride Extended-release Tablets USP (XL) 300 mg by AvPAK. The label indicates once daily dosage, Rx only, and contains 30 tablets in unit dose packaging (6 x 5). It includes warnings about drug interactions, pharmacist dispensing instructions, storage conditions, and proper dosage guidelines.*
FDA Label Image

Image (A4f3a9c2 27ba 4de5 Ad30 347e392d8045 01)

Image (A4f3a9c2 27ba 4de5 Ad30 347e392d8045 01)
Chemical structure of Bupropion Hydrochloride depicting its molecular arrangement including a chlorophenyl group, ketone, amine, and tert-butyl substituents with 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.