Aurobindo Pharma recalls 0.5mg Rasagiline Tablets (30-count) due to failed dissolution testing. This may affect drug effectiveness. Check NDC 0378-1270-93 and lot 3112444.
Failed dissolution specifications - results obtained were below spec average.
Aurobindo Pharma is recalling 0.5mg Rasagiline Tablets (30-count) because they failed dissolution testing. This could mean the medication doesn't work as intended, so affected users should contact their doctor.
The tablets failed dissolution testing, meaning they don't dissolve properly in the body. This could lead to the medication not working as intended, but it does not cause immediate harm or injury.
People with a prescription for Rasagiline Tablets 0.5mg, 30-count bottles from Mylan Pharmaceuticals. Those who have the specific NDC 0378-1270-93 lot 3112444 are most at risk.
Check for the NDC code 0378-1270-93 on the bottle label. The lot number 3112444 and expiration date 8/2023 are also specific to this recall.
Talk to your healthcare provider about the recall and possible next steps for your medication.
No, the recall is for potential reduced effectiveness, not immediate safety risks.
Look for the NDC code 0378-1270-93 and lot number 3112444 on the bottle label.
Contact your doctor for advice on whether to continue using the medication.
We’ve drafted a message you can send Aurobindo Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-1171-2023 — Aurobindo Pharma Aurobindo Pharma Hello, I own a Aurobindo Pharma that is covered by recall D-1171-2023 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.
