Bupropion Hydrochloride Tablet, Extended Release
Product Images NDC 82009-052
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This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Bupropion Hydrochloride (NDC 82009-052). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Quallent Pharmaceuticals Health Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Bupropion Hydrochloride Extended-release Tablets Usp (xl)150 mgrx Onlybottle Of 500 Tablets (D4972b84 9442 42dc B5c7 3dae4833203a 02)
This is a description for NDC 82009-051-05, a medication containing bupropion hydrochloride in the form of extended-release tablets. The tablets are to be taken once daily or as directed by a physician. It is important to note a warning against using other medicines containing bupropion hydrochloride with this medication. The pharmacist is instructed to dispense a medication guide to each patient. The medication should be stored at a temperature of 25°C (77°F), with permitted excursions to 15° to 30°C (59° to 86°F). For additional dosing information, the package insert should be consulted. The medication is manufactured by Quallent Pharmaceuticals and distributed by Lupin Limited.*
Bupropion Hydrochloride Extended Release Tablets Usp (xl) 300 mgrx Onlybottle Of 500 Tablets (D4972b84 9442 42dc B5c7 3dae4833203a 03)
This is a description for a medication called buPROPion Hydrochloride Extended-release Tablets USP (XL). It is a once-daily medication that contains bupropion hydrochloride in a 300mg dosage. The medication guide should be provided to each patient by the pharmacist. The tablets should be stored at a temperature between 15° to 30°C (59° to 86°F). For more information, including the Medication Guide, visit the website www.quallentpharmaceuticals.com. The medication is manufactured by Quallent Pharmaceuticals and Health LLC Lupin Limited. The product code is GO/DRUGS/654.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.