Sun Pharmaceutical recalls 70mg lisdexamfetamine capsules with failed dissolution tests. This may affect drug stability and safety. Check NDC 57664-052-88 for affected lots.
Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 12-month long term stability station (25¿C, 60%RH) for Lisdexamfetamine dimesylate capsules.
Sun Pharmaceutical is recalling 70mg lisdexamfetamine dimesylate capsules due to failed dissolution tests at 12 months. This could mean the medication doesn't work properly over time, potentially affecting treatment effectiveness.
The capsules failed dissolution tests during long-term stability testing, meaning they may not release the medication properly over time. This could lead to inconsistent dosing or reduced effectiveness of the medication.
Prescription users of the 70mg lisdexamfetamine capsules with NDC 57664-052-88. People who have the specific lot numbers AD48712 (expiring 4/30/2026) or AD50898 (expiring 5/31/2026) are most at risk.
Check the product label for NDC 57664-052-88. Look for lot numbers AD48712 (expiring 4/30/2026) or AD50898 (expiring 5/31/2026). The product is prescription-only and sold in 100-count bottles.
Look for the NDC code 57664-052-88 and lot numbers AD48712 or AD50898 on the capsule packaging.
The recall is due to failed dissolution tests, which could affect medication effectiveness. The product is still safe to use but may not work as intended over time.
Check the product label for NDC 57664-052-88 and lot numbers AD48712 (expiring 4/30/2026) or AD50898 (expiring 5/31/2026).
The recall does not specify a remedy, so contact your doctor or pharmacist for advice on next steps.
We’ve drafted a message you can send Sun Pharmaceutical to request your refund or repair — edit it as you like.
Subject: Recall D-0150-2026 — Sun Pharmaceutical Sun Pharmaceutical Hello, I own a Sun Pharmaceutical that is covered by recall D-0150-2026 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.
