Bupropion Hydrochloride Tablet, Film Coated
Product Images NDC 60760-781

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Bupropion Hydrochloride (NDC 60760-781). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by St. Mary's Medical Park Pharmacy, 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

781-30 (Bupropion 60760 781 30)

Label for Bupropion Hydrochloride tablets, USP 100 mg, film-coated, oral dosage form. The label indicates a quantity of 30 tablets per package. Manufactured by Apotex Inc., Toronto, Ontario, Canada, and packaged by St. Mary's Medical Park Pharmacy, Oro Valley, AZ. Storage instructions specify controlled room temperature between 15°-30°C (59°-86°F). The label includes placeholders for lot number and expiration date, and a 2D barcode with numeric codes.*

FDA Label Image

Structure (Structure)

Chemical structure diagram of Bupropion Hydrochloride displaying its characteristic molecular groups, including a chlorophenyl ring and various substituents indicating its chemical composition.*

* 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.