Bupropion Hydrochloride
Product Images NDC 63304-724

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Bupropion Hydrochloride (NDC 63304-724). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, Inc., 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

Structure (Bupropion 01)

Chemical structure diagram of bupropion hydrochloride showing its molecular framework including the chlorophenyl group and tertiary amine with a hydrochloride salt.*

FDA Label Image

Pdp-1 (Bupropion 02)

Label for Bupropion Hydrochloride 300 mg extended-release tablets, USP (XL) manufactured by Sun Pharmaceutical Industries, Inc. The bottle contains 30 tablets for once-daily use. The label includes dosage instructions, storage conditions, warnings, and manufacturer details from Sun Pharmaceutical Industries Limited in India and Cranbury, NJ in the U.S.*

FDA Label Image

Pdp-2 (Bupropion 03)

Label for Bupropion Hydrochloride Extended-Release Tablets, USP (XL) 300 mg by Sun Pharmaceutical Industries, Inc. The label shows the proprietary name, strength, dosage form, quantity of 90 tablets, Rx only status, NDC 63304-724-90, and includes warnings and storage instructions. The label also features barcodes and manufacturer information.*

FDA Label Image

Pdp-3 (Bupropion 04)

Label for buPROPion Hydrochloride Extended-Release Tablets USP (XL) 300 mg by Sun Pharmaceutical Industries Limited, distributed by Sun Pharmaceutical Industries, Inc. The label states a 500 tablet count and includes usage warnings, dosage instructions, storage conditions, and trademark information for Zyban. The product NDC is 63304-724.*

* 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.