Bupropion Hydrochloride Extended Release
Product Images NDC 10135-703

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Bupropion Hydrochloride Extended Release (NDC 10135-703). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Marlex Pharmaceuticals 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

Structural Formula (Bupropion Hydrochloride Extended Release Tablets 01)

Chemical structure of Bupropion Hydrochloride showing the molecular arrangement including a chlorophenyl group, a ketone, and a tertiary amine with hydrochloride.*

FDA Label Image

Ndc 10135-0703-3030 Tablets Bupropion HCl Er Tablets 150 mg Rx Only (Bupropion Hydrochloride Extended Release Tablets 02)

Packaging label for Bupropion Hydrochloride Extended Release Tablets 150 mg, XL. The label shows it is a once-daily prescription medication containing 30 tablets. The labeler is Marlex Pharmaceuticals Inc, New Castle, DE. The label includes dosing information, storage instructions, and a warning about use with other bupropion-containing medicines.*

FDA Label Image

Ndc 10135-0703-9090 Tablets Bupropion HCl Er Tablets 150 mg Rx Only (Bupropion Hydrochloride Extended Release Tablets 03)

Label for Bupropion Hydrochloride Extended-Release Tablets, XL, 150 mg strength, provided by Marlex Pharmaceuticals Inc. The label indicates a package of 90 tablets for once-daily use. It includes usual dosage instructions, storage conditions, and warnings about concurrent use with Zybam or other bupropion-containing medicines. The product is marked Rx only and has a barcode on the right side.*

FDA Label Image

Ndc 10135-0703-05500 Tablets Bupropion HCl Er Tablets 150 mg Rx Only (Bupropion Hydrochloride Extended Release Tablets 04)

Label for Bupropion Hydrochloride Extended Release Tablets, 150 mg, by Marlex Pharmaceuticals, Inc. The label states the tablet is once-daily, extended-release, with a quantity of 500 tablets. It includes dosage and storage information, a warning not to combine with certain medicines, pharmacist instructions, and manufacturer details with a barcode.*

FDA Label Image

Ndc 10135-0704-3030 Tablets Bupropion HCl Er Tablets 300 mg Rx Only (Bupropion Hydrochloride Extended Release Tablets 05)

Label for Bupropion Hydrochloride Extended-Release Tablets, 300 mg, XL (extra-long) from Marlex Pharmaceuticals Inc. The label indicates a 30-tablet package, with instructions and warnings visible including dosage guidance, storage conditions, and pharmacist dispensing instructions. The NDC number and barcode are also shown.*

FDA Label Image

Ndc 10135-0704-9090 Tablets Bupropion HCl Er Tablets 300 mg Rx Only (Bupropion Hydrochloride Extended Release Tablets 06)

The label is for Bupropion Hydrochloride Extended Release Tablets XL, 300 mg strength, by Marlex Pharmaceuticals Inc. It is for a 90-tablet bottle. The label includes dosage instructions, warnings, pharmacist dispensing advice, and storage conditions. It also features a barcode and an NDC number 10135-0704-90.*

FDA Label Image

Ndc 10135-0704-05500 Tablets Bupropion HCl Er Tablets 300 mg Rx Only (Bupropion Hydrochloride Extended Release Tablets 07)

Label for Bupropion Hydrochloride Extended-Release Tablets (XL) 300 mg by Marlex Pharmaceuticals Inc. The label states the product is a once-daily prescription medication, packaged as 500 tablets. It includes dosage and storage information, warnings, and manufacturer details, along with a barcode and the NDC 10135-0704-05.*

* 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.