Sun Pharmaceutical recalls 150mg buPROPrion Hydrochloride Extended-Release Tablets (NDC 47335-737-86) that failed dissolution testing during stability checks. This could affect medication effectiveness.
Failed Dissolution Specifications; during stability testing
Sun Pharmaceutical is recalling 150mg buPROPrion XR tablets that failed dissolution testing during stability checks. This means the medication might not work as intended, so affected users should contact their doctor for alternatives.
The tablets failed dissolution testing during stability checks, meaning they may not release medication properly over time. This could lead to inconsistent dosing or reduced effectiveness of the medication.
People with prescriptions for buPROPrion XR 150mg tablets manufactured by Sun Pharmaceutical in India and distributed by Sun Pharmaceutical Industries, Inc. in the US. Those who have the specific lot numbers or expiration dates listed are most at risk.
Check your prescription label for 'buPROPrion Hydrochloride Extended-Release Tablets, USP (SR) 150 mg, 60 Tablets, Rx Only'. Look for lot numbers HAC2240A (expiring May 2023) or HAC3162A (expiring July 2023).
Review your prescription label for the specific lot numbers HAC2240A or HAC3162A and expiration dates.
The tablets failed dissolution testing during stability checks, which could mean they don't release medication properly.
No, but you should contact your doctor for alternatives since the medication might not work as intended.
Check your prescription label for the specific lot numbers and expiration dates. If you have the recalled lot numbers, contact your doctor for alternatives.
We’ve drafted a message you can send Sun Pharmaceutical to request your refund or repair — edit it as you like.
Subject: Recall D-0761-2023 — Sun Pharmaceutical Sun Pharmaceutical Hello, I own a Sun Pharmaceutical that is covered by recall D-0761-2023 from Sun Pharmaceutical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
