Wellbutrin Xl
Product Images NDC 54868-4935

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 Wellbutrin Xl (NDC 54868-4935). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Physicians Total Care, 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.

Product Images & Figures Index

FDA Label Image

Image Of 300 mg Package Label (4935)

Image Of 300 mg Package Label (4935)
The image shows a white pharmaceutical label for WELLBUTRIN XL 300MG tablets. It displays the NDC number 54868-4935-0 and identifies Physicians Total Care, Inc. as the distributor in Tulsa, OK. The label includes a lot number, expiration date, manufacturer information (BioRail Corp International, Mississauga, Ontario), and a barcode.*
FDA Label Image

Image Of 150 mg Package Label (5010)

Image Of 150 mg Package Label (5010)
WELLBUTRIN XL 150 mg extended-release tablets label by Physicians Total Care, Inc., showing that the package contains 30 tablets. The active ingredient is bupropion hydrochloride. The label includes dosage form information, federal caution about prescription dispensing, and storage instructions. It also provides a lot number, expiration date, and manufacturer details.*
FDA Label Image

Chemical Structure (Wellbutrin Xl 01)

Chemical Structure (Wellbutrin Xl 01)
Chemical structure of the active ingredient in WELLBUTRIN XL is depicted. The formula includes a chlorinated aromatic ring, methyl ester, and hydrochloride component, representing the molecular layout relevant to the drug.*

* 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.