Novitium Pharma recalls 1000-count Digoxin tablets (125mcg) due to cross contamination with mycophenolate mofetil. This may cause unintended medication interactions. Contact for return instructions.
Cross Contamination with Other Products:(mycophenolate mofetil).
Novitium Pharma is recalling 1000-count Digoxin tablets (125mcg) because they may have been contaminated with mycophenolate mofetil. This cross-contamination could lead to unintended medication interactions if taken by patients who require Digoxin.
The tablets may contain traces of mycophenolate mofetil, a medication used for immunosuppression. If taken by someone who requires Digoxin, this could cause unintended interactions with their treatment.
Patients prescribed Digoxin tablets by a doctor are affected. Those with specific medical conditions requiring precise medication dosing are at higher risk.
Check for the 1000-count bottle labeled 'Digoxin Tablets, USP 125mcg (0.125 mg)' manufactured by Novitium Pharma LLC. The lot number M23172A with expiration date 01/31/2025 is also specific to this recall.
Verify the product label matches the recall description: 1000-count bottle, 125mcg tablets, manufactured by Novitium Pharma LLC, lot M23172A, expiring 01/31/2025.
The recall is for potential cross-contamination with mycophenolate mofetil, which could cause unintended medication interactions. However, the risk level is low as the contamination is not confirmed to cause serious harm.
Check for the 1000-count bottle labeled 'Digoxin Tablets, USP 125mcg (0.125 mg)' manufactured by Novitium Pharma LLC with lot number M23172A and expiration date 01/31/2025.
The recall does not specify a remedy, so contact Novitium Pharma directly for guidance on next steps.
We’ve drafted a message you can send Novitium Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0389-2024 — Novitium Pharma Novitium Pharma Hello, I own a Novitium Pharma that is covered by recall D-0389-2024 from Novitium 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.
