Novitium Pharma recalls 100-count Digoxin tablets (62.5 mcg) due to failed impurities tests. This could cause serious health issues if taken. Contact the manufacturer for details.
Failed Impurities/Degradation Specifications
Novitium Pharma is recalling 100-count Digoxin tablets (62.5 mcg) because they failed impurities and degradation tests. This could lead to serious health problems if taken without proper quality control.
The tablets failed impurities and degradation specifications, meaning they may contain harmful substances or break down into unsafe compounds. This could cause serious health issues if taken as directed.
Prescription drug users who have the specific 100-count Digoxin tablets with NDC 70954-200-10 and lot number M23011A. People with heart conditions requiring Digoxin are most at risk.
Check for the 100-count bottle labeled 'Digoxin Tablets, USP 62.5 mcg (0.0625 mg)', manufactured by Novitium Pharma LLC, with NDC 70954-200-10 and lot number M23011A.
Look for the NDC code 70954-200-10 and lot number M23011A on the bottle label.
The official recall does not state if the product is safe to use; it was recalled due to failed impurities and degradation tests.
The recall record does not mention any remedy or replacement options.
The recall record does not specify actions for affected users beyond checking product details.
We’ve drafted a message you can send Novitium Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0443-2024 — Novitium Pharma Novitium Pharma Hello, I own a Novitium Pharma that is covered by recall D-0443-2024 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.
