Bupropion Hydrochloride (xl) Tablet, Extended Release
Product Images NDC 0527-2430

9 FDA label images from Lannett Company Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Bupropion Hydrochloride (xl) (NDC 0527-2430). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lannett Company 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

150mg1000s (150mg1000s)

150mg1000s (150mg1000s)
Label for Bupropion Hydrochloride Extended-Release Tablets USP (XL) 150 mg by Lannett Company Inc. The label indicates each extended-release tablet contains 150 mg bupropion hydrochloride. It includes dosage storage instructions, a warning against use with Zybun and related drugs, and states the package contains 1000 tablets. Manufactured in China, the label features a barcode and the Lannett logo.*
FDA Label Image

150mg30s (150mg30s)

150mg30s (150mg30s)
Label for Bupropion Hydrochloride Extended-Release Tablets USP (XL) 150 mg, manufactured by Lannett Company Inc. It shows the dosage form as oral extended-release tablets, package containing 30 tablets, and storage instructions. The label includes a warning about not using in combination with Zyclara or other bupropion HCl-containing medicines and states distribution by Lannett Company Inc., Philadelphia, PA.*
FDA Label Image

150mg500s (150mg500s)

150mg500s (150mg500s)
Label for Bupropion Hydrochloride Extended-Release Tablets, USP (XL) 150 mg by Lannett Company Inc. The product is presented as an oral extended-release tablet, with a package count of 500 tablets. The label includes dosage instructions, storage conditions, warnings against combining with Zyban or other bupropion products, and manufacturer information from Hangzhou Minsheng Binjiang Pharmaceutical Co., Ltd. It also features the NDC number 0527-2415-41 and a barcode.*
FDA Label Image

150mg90s (150mg90s)

150mg90s (150mg90s)
Label for Bupropion Hydrochloride Extended-Release Tablets, USP (XL) 150 mg oral tablets by Lannett Company Inc. The label states the product is for once-daily use and contains 90 tablets. It includes dosage information, storage conditions, and warnings about drug interactions. The product is manufactured in China and distributed by Lannett Company Inc.*
FDA Label Image

300mg1000s (300mg1000s)

300mg1000s (300mg1000s)
Label for Bupropion Hydrochloride Extended-Release Tablets, USP (XL) 300 mg by Lannett Company Inc. The label indicates one tablet extended-release dosage, contains 1000 tablets, and is marked for once-daily use. It includes storage instructions, a warning against use with Zyban or other bupropion-containing medicines, and pharmacist dispensing instructions. The product is manufactured in China.*
FDA Label Image

300mg30s (300mg30s)

300mg30s (300mg30s)
Bupropion hydrochloride Extended-Release Tablets, USP (XL) 300 mg oral tablets packaging label. The label shows the product name, strength, dosage form, Dosing directions, storage instructions, warning against use with Zybam, and manufacturer information for Lannett Company Inc. The package contains 30 tablets.*
FDA Label Image

300mg500s (300mg500s)

300mg500s (300mg500s)
Label for Bupropion Hydrochloride Extended-Release Tablets, USP (XL) 300 mg. The tablet is for once-daily oral use and dispensed by prescription only. The label highlights the 300 mg strength and the extended-release formulation. It indicates storage conditions at 25°C (77°F) with permitted excursions, warnings about use with Zyban, and instructs pharmacists to dispense the enclosed Medication Guide. Manufactured by Hangzhou Minsheng Binjiang Pharmaceutical Co., Ltd and distributed by Lannett Company Inc. Label shows NDC code 0527-2430-41 and a bottle count of 500 tablets.*
FDA Label Image

300mg90s (300mg90s)

300mg90s (300mg90s)
Bupropion hydrochloride Extended-Release Tablets, USP (XL) 300 mg oral tablets are shown on a label by Lannett Company Inc. The label states the product is for once-daily use and contains 90 tablets. It includes storage instructions, a warning against combining with Zybun or similar medicines, and manufacturer information from Hangzhou Minsheng Binjiang Pharmaceutical Co., China.*
FDA Label Image

Image Description (Image)

Image Description (Image)
Chemical structure of Bupropion hydrochloride depicting its molecular arrangement, including a chlorophenyl ring, a tert-butyl group, and the hydrochloride component as indicated by HCl.*

* 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.