Wellbutrin Xl
Product Images NDC 21695-138

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Wellbutrin Xl (NDC 21695-138). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rebel Distributors Corp, 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 (Fdd1fa5e 9dbf 4951 A8e9 33d06e05bdba 01)

Chemical structure of Wellbutrin XL showing its molecular framework including key groups such as methyl, ethyl, chlorine, and hydrochloride components as typically represented in the chemical diagram.*

FDA Label Image

Wellbutrin Xl 150mg (Fdd1fa5e 9dbf 4951 A8e9 33d06e05bdba 02)

Packaging label for Wellbutrin XL 150 mg ER tablets, containing 30 extended-release tablets. The label displays the Proprietary name, strength, dosage form, and quantity, with a note that each ER tablet contains 150 mg of bupropion HCl. The labeler is Rebel Distributors Corp with a distributor named Physician Partner, located in Thousand Oaks, CA. Additional warnings and storage conditions are provided on the label.*

FDA Label Image

Wellbutrin Xl 300mg (Fdd1fa5e 9dbf 4951 A8e9 33d06e05bdba 03)

Label for Wellbutrin XL 300 mg extended-release tablets, package size of 30 tablets. The label shows the product name, strength, dosage form, and notes that each ER tablet contains 300 mg of bupropion hydrochloride. The label includes the NDC 21696-138-30, manufacturer information (Biovail Corporation, Mississauga, Canada), and distributor information (Physician Partner, Thousand Oaks, CA). The tablet description notes yellow, round tablets with specific imprinting.*

* 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.