Bupropion Hydrochloride Tablet, Extended Release
Product Images NDC 33342-527

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Bupropion Hydrochloride (NDC 33342-527). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Macleods Pharmaceuticals Limited, 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

112 (Bupripion Tablet Structure)

Chemical structure of Bupropion Hydrochloride showing its molecular components including the chlorophenyl group, and the hydrochloride salt indicated by 3 HCl.*

FDA Label Image

112 (Bupropion 100mg 100s)

Label for Bupropion Hydrochloride Extended-Release Tablets, USP (SR) 100 mg by Macleods Pharmaceuticals Limited. The label indicates the product is for oral use, with a 100-tablet count. It includes storage instructions, a warning against use with Zyban or other bupropion-containing medicines, and manufacturing information by Macleods Pharma USA and Macleods Pharmaceuticals Ltd, India.*

FDA Label Image

112 (Bupropion 100mg 500s)

Label for Bupropion Hydrochloride Extended-Release Tablets USP (SR) 100 mg by Macleods Pharmaceuticals Limited. The label states this is a twice-a-day dosage after initial titration, with 500 tablets per bottle. It includes storage instructions and a warning not to use with medicines containing bupropion hydrochloride. The product is manufactured in India for Macleods Pharma USA, Inc.*

FDA Label Image

112 (Bupropion 100mg 60s)

Label for Bupropion Hydrochloride Extended-Release Tablets USP (SR) 100 mg by Macleods Pharmaceuticals Limited. The label states the dosage form as extended-release tablets, 100 mg strength, with 60 tablets in the container. It includes storage instructions and trademark acknowledgment for Zyban. Manufactured for Macleods Pharma USA, Inc., Princeton, NJ, with manufacturing details in India.*

FDA Label Image

112 (Bupropion 150mg 100s)

Label for Bupropion Hydrochloride Extended-Release Tablets USP (SR) 150 mg by Macleods Pharmaceuticals Limited. The label states it is for twice-a-day dosing after initial titration and includes storage instructions, manufacturer details, and a 100-tablet count. It features warning and pharmacist directions alongside barcodes and a designated printing area.*

FDA Label Image

112 (Bupropion 150mg 500s)

Label for Bupropion Hydrochloride Extended-Release Tablets, USP (SR), 150 mg strength. The label shows the product is manufactured by Macleods Pharmaceuticals Limited and labeled for Macleods Pharma USA, Inc. It indicates a quantity of 500 tablets and includes storage instructions, trademark notice for Zyban, and usage warnings. The tablet is for oral use with extended-release formulation.*

FDA Label Image

112 (Bupropion 150mg 90s)

Label for Bupropion Hydrochloride Extended-Release Tablets, USP (SR) 150 mg, manufactured by Macleods Pharmaceuticals Ltd. and Macleods Pharma USA, Inc. This oral prescription drug is packaged as 90 tablets. The label includes storage instructions and a warning about drug interactions.*

FDA Label Image

112 (Bupropion 200mg 100s)

Label for Bupropion Hydrochloride Extended-Release Tablets, USP (SR) 200 mg by Macleods Pharmaceuticals Limited. The label indicates a 100-tablet package with dosage instructions as Twice-A-Day after initial titration. It includes storage instructions and a manufacturer address for Macleods Pharma USA, Inc., Princeton, NJ, and manufacturing details from India.*

FDA Label Image

112 (Bupropion 200mg 60s)

Label of Bupropion Hydrochloride Extended-Release Tablets, USP (SR) 200 mg by Macleods Pharmaceuticals Limited. The label indicates a 60 tablet count and notes the product is manufactured for Macleods Pharma USA, Inc. It includes storage instructions, a warning about use with Zyban, and dosage form as extended-release oral tablets.*

* 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.