Bupropion Hydrochloride Tablet, Extended Release
Product Images NDC 72189-124

4 FDA label images from Direct Rx · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Bupropion Hydrochloride (NDC 72189-124). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct Rx, 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

057 (057 30)

057 (057 30)
Packaging label for Bupropion HCl SR 100 mg extended-release oral tablets, 30 count. The label indicates the product is generic for Wellbutrin and is packaged and distributed by Direct Rx. The label includes lot number and expiration date information, with a yellow highlighted section showing the strength and tablet count.*
FDA Label Image

72189 124 30

72189 124 30
Label for BUPROPION HCL ER (XL) 300 mg extended release tablets, containing 30 tablets per bottle. The label indicates it is generic for Wellbutrin XL and manufactured or distributed by DIRECT RX. The label includes lot sample information and expiration date details.*
FDA Label Image

72189 134 30

72189 134 30
Packaging label for Bupropion HCL Extended Release (XL) 150 mg oral tablets. The label indicates a quantity of 30 tablets per container. It notes the product is a generic for Wellbutrin XL and includes lot and expiration details. The labeler shown is DIRECT Rx, with packaging location in Dawsonville, GA.*
FDA Label Image

72189 134 90

72189 134 90
BUPROPION HYDROCHLORIDE extended-release (XL) 150 mg oral tablet label, containing 90 tablets. The label indicates it is a generic for WELLBUTRIN XL, with each extended-release tablet containing 150 mg bupropion hydrochloride USP. Packaged by DIRECT RX, the label includes NDC 72189-134-90 and relevant manufacturing and discard information.*

* 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.