Bupropion Hydrochloride Tablet, Extended Release
Product Images NDC 71205-968

4 FDA label images from Proficient Rx Lp · 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 71205-968). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

71205-967-30 (Bot 150mg 30count)

71205-967-30 (Bot 150mg 30count)
Label for Bupropion HCl 150 mg extended-release (XL) tablets, once daily, in a 30-count package. The label includes the ProficientRx logo and states the active ingredient bupropion hydrochloride per tablet. Manufactured by TWI Pharmaceuticals, Taiwan, the label advises keeping medication out of children's reach and storing at 20°-25°C. The tablet is described as white film-coated with "T101" on one side.*
FDA Label Image

71205-968-30 (Bot 300mg 30count)

71205-968-30 (Bot 300mg 30count)
Label for Bupropion Hydrochloride (XL) 300 mg extended-release tablets by Proficient Rx LP. The label indicates a 30-count package, with each white film-coated tablet imprinted with "T102" on one side. The manufacturer is TWi Pharmaceuticals, Inc., Taiwan. The label includes storage instructions and warnings.*
FDA Label Image

Image Description (Bupropion Hydrochloride Sr 1)

Image Description (Bupropion Hydrochloride Sr 1)
Chemical structure of bupropion hydrochloride showing a chlorophenyl ring bonded to a ketone and a tert-butyl group, with the hydrochloride (HCl) salt indicated.*
FDA Label Image

* 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.