Bupropion Hydrochloride Tablet, Film Coated, Extended Release
Product Images NDC 50228-145

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Bupropion Hydrochloride (NDC 50228-145). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sciegen 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

Bupropion-150mg-30tab (Bupropion 150mg 30tab)

Bupropion-150mg-30tab (Bupropion 150mg 30tab)
Label for buPROPion Hydrochloride Extended-Release Tablets USP (XL) 150 mg, film-coated oral tablets. The label indicates a 30 count bottle, manufactured by ScieGen Pharmaceuticals, Inc. Storage instructions and dosage warnings are included. The label also displays an NDC barcode and specifies prescription use only.*
FDA Label Image

Buproion-150mg-500tab (Bupropion 150mg 500tab)

Buproion-150mg-500tab (Bupropion 150mg 500tab)
Label for Bupropion Hydrochloride extended-release tablets, USP (XL) 150 mg by ScieGen Pharmaceuticals, Inc. The label states the product is once-daily and contains 500 tablets. Storage and usage instructions, along with a warning about co-use with Zyban, are included. A barcode and the ScieGen logo are also visible.*
FDA Label Image

Bupropion 150mg 90tab

Bupropion 150mg 90tab
Label for buPROPion Hydrochloride Extended-Release Tablets, USP (XL) 150 mg oral film-coated tablets by ScieGen Pharmaceuticals, Inc. The label indicates once-daily dosing, contains 90 tablets per bottle, and includes storage instructions and a medication guide warning about drug interactions. NDC 50228-144-90 is shown alongside a barcode.*
FDA Label Image

Buproion-300mg-30tab (Bupropion 300mg 30tab)

Buproion-300mg-30tab (Bupropion 300mg 30tab)
Label for Bupropion Hydrochloride (XL) extended-release tablets, 300 mg strength. The label indicates a once-daily oral dosage form with 30 tablets per package. It is manufactured by ScieGen Pharmaceuticals, Inc. The label includes dosage instructions, storage conditions, a barcode, and a warning regarding use with Zyban or other bupropion products.*
FDA Label Image

Buproion-300mg-500tab (Bupropion 300mg 500tab)

Buproion-300mg-500tab (Bupropion 300mg 500tab)
Label for Bupropion Hydrochloride Extended-Release Tablets, USP (XL), 300 mg strength. The label indicates a package containing 500 film-coated extended-release tablets for oral use. It includes dosage directions, storage instructions, a warning against use with Zyban or other bupropion hydrochloride products, and states the product is manufactured by ScieGen Pharmaceuticals, Inc.*
FDA Label Image

Bupropion 300mg 90tab

Bupropion 300mg 90tab
Label for Bupropion Hydrochloride (XL) Extended-Release Tablets, 300 mg strength, oral film-coated tablets by ScieGen Pharmaceuticals, Inc. The label states once-daily use, includes a barcode, storage instructions at 25°C, and a warning against use with Zyban or other bupropion hydrochloride medicines. The package contains 90 tablets with Rx only designation.*
FDA Label Image

Bupropion Hydrochloride Chemical Structure (Bupropion Hydrochloride Sr 1)

Bupropion Hydrochloride Chemical Structure (Bupropion Hydrochloride Sr 1)
Chemical structure of bupropion hydrochloride. The structure shows a benzene ring substituted with chlorine, connected to a side chain including an amine group with three methyl groups and a ketone functional group, with the hydrochloride component indicated.*

* 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.