Sun Pharmaceutical recalls 500mg Divalproex Sodium Delayed-Release Tablets due to failed dissolution testing. This may affect medication effectiveness. Contact Sun Pharmaceutical for details.
Failed Dissolution Specifications: Failure occurred during routine stability testing of dissolution test.
Sun Pharmaceutical is recalling 50:000mg Divalproex Sodium Delayed-Release Tablets because they failed dissolution testing during stability checks. This could mean the medication doesn't work as intended when taken.
The tablets failed dissolution testing during routine stability checks. This means the medication may not release properly in the body, potentially reducing effectiveness. However, the recall does not indicate a risk of injury or serious harm.
Prescription patients who received these specific tablets from Sun Pharmaceutical. Those with a prescription for this medication are most at risk.
Check for the product name 'Divalproex Sodium Delayed-Release Tablets, USP 500mg, Rx Only, 100 Tablets'. Look for the lot number HAC1312A and expiration date 05/2024 on the packaging.
Look for the lot number HAC1312A and expiration date 05/2024 on the packaging.
The recall is due to failed dissolution testing, which may affect medication effectiveness but does not indicate a risk of injury or serious harm.
Check for the product name 'Divalproex Sodium Delayed-Release Tablets, USP 500mg, Rx Only, 100 Tablets' with lot number HAC1312A and expiration date 05/2024.
The recall does not specify a remedy, so contact Sun Pharmaceutical directly for guidance.
We’ve drafted a message you can send Sun Pharmaceutical to request your refund or repair — edit it as you like.
Subject: Recall D-1291-2022 — Sun Pharmaceutical Sun Pharmaceutical Hello, I own a Sun Pharmaceutical that is covered by recall D-1291-2022 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.
