Bupropion Hydrochloride
Product Images NDC 64725-0737

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Bupropion Hydrochloride (NDC 64725-0737). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Tya Pharmaceuticals, 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

Label Image (64725 0736)

Packaging label for Bupropion hydrochloride extended-release (ER) 100 mg tablets, 100 count bottle. The label indicates the product is manufactured by Sun Pharma and repackaged by TYA Pharmaceuticals in Tallahassee, FL. Includes an NDC number and instructions to see the package insert for dosing information.*

FDA Label Image

Label Image (64725 0737)

Label for Bupropion hydrochloride ER (SR) 150 mg tablets, with 100 count. It indicates prescription use only, manufactured by Sun Pharma, and repackaged by TYA Pharmaceuticals in Tallahassee, FL. The lot number and expiration date fields are marked with placeholders. A barcode is present along with a note to see the package insert for dosing information.*

FDA Label Image

Chemical-structure (Bupropionsr Str)

Chemical structure of bupropion hydrochloride displaying a chlorophenyl ring with attached ketone and tert-butylamine groups, alongside the hydrochloride component.*

* 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.