Sun Pharmaceutical recalls 0.125mg Clonazepam orally disintegrating tablets due to oversized tablets found in bottles. This may affect prescription medication safety.
Failed Tablet/Capsule Specification; oversized tablet found in a bottle
Sun Pharmaceutical is recalling 0.125mg Clonazepam orally disintegrating tablets because some bottles contain oversized tablets. This could cause incorrect dosing if taken.
The tablets contain oversized tablets that may not dissolve properly in the mouth. This could lead to incorrect dosing if taken as prescribed.
Prescription patients who received these specific tablets from Sun Pharmaceutical. Those with the NDC 57664-783-68 lot number MHC1430A are most at risk.
Check for the NDC code 57664-783-68 and lot number MHC1430A on the bottle. The product was manufactured in India and distributed in the US by Sun Pharmaceutical.
Look for the NDC code 57664-783-68 and lot number MHC1430A on the bottle.
The recall states oversized tablets were found, which could lead to incorrect dosing. The product is not safe to use as recalled.
Check for NDC code 57664-783-68 and lot number MHC1430A on the bottle.
The recall does not specify a remedy, so contact Sun Pharmaceutical 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-1155-2022 — Sun Pharmaceutical Sun Pharmaceutical Hello, I own a Sun Pharmaceutical that is covered by recall D-1155-2022 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.
