Aurobindo Pharma USA Inc. recalls 6.25 mg Carvedilol tablets (NDC 65862-143-05) due to failed impurities and degradation specifications. This Rx-only medication was distributed from 279 Princeton-Hightstown Road, East Windsor, NJ.
Failed Impurities/Degradation Specifications
Aurobindo Pharma is recalling 6.25 mg Carvedilol tablets (500-count bottles) because they failed impurities and degradation specifications. This means the medication may not be safe for use as intended, though the recall does not specify injury risks or remedies.
The tablets failed impurities and degradation specifications, which means they may contain harmful substances or break down in a way that affects safety. This could lead to unexpected health effects, but the recall does not specify what those effects are or how serious they might be.
Prescription drug users who have the 6.25 mg Carvedilol tablets (NDC 65862-143-05) from Aurobindo Pharma. People with this medication are most at risk if they use it without following the recall instructions.
Check for the 6.25 mg Carvedilol tablets (500-count bottle) with NDC 65862-143-05. This product was distributed by Aurobindo Pharma USA Inc. from 279 Princeton-Hightstown Road, East Windsor, NJ, and made in India.
Look for the NDC code 65862-143-05 on the bottle label to confirm if you have the recalled product.
The recall states the tablets failed impurities and degradation specifications, but does not specify injury risks or remedies.
Check for the 6.25 mg Carvedilol tablets (500-count bottle) with NDC 65862-143-05, which were distributed by Aurobindo Pharma USA Inc. from 279 Princeton-Hightstown Road, East Windsor, NJ.
The recall does not provide specific action steps or remedies for affected users.
We’ve drafted a message you can send Aurobindo Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0263-2022 — Aurobindo Pharma Aurobindo Pharma Hello, I own a Aurobindo Pharma that is covered by recall D-0263-2022 from Aurobindo Pharma. 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.
