Biocon Pharma recalls 40mg Atorvastatin Calcium Tablets due to failed dissolution specifications. This may affect medication effectiveness. Contact for details.
Failed dissolution specifications: lower than specifications
Biocon Pharma is recalling 1000-count bottles of 40mg Atorvastatin Calcium Tablets because they didn't dissolve properly as required. This could mean the medication isn't working correctly for people taking it.
The tablets didn't dissolve at the required rate, which could lead to inconsistent medication levels in the body. This might reduce the drug's effectiveness for managing cholesterol.
People with prescriptions for this medication are affected. Those who have the specific bottle with NDC 70377-079-13 are most at risk.
Check for the 1000-count bottle labeled 'Atorvastatin Calcium Tablets USP 40 mg, Rx Only'. The NDC code is 70377-079-13 and it was manufactured in India with lot number AVC24035.
Look for the NDC code 70377-079-13 on the bottle label to confirm if it's recalled.
The recall is due to failed dissolution specifications, which may affect medication effectiveness but does not indicate immediate danger.
Check for the NDC code 70377-079-13 on the bottle label, which is specific to this recall.
The recall does not include a specific remedy, so contact Biocon Pharma for further instructions.
We’ve drafted a message you can send Biocon Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0306-2025 — Biocon Pharma Biocon Pharma Hello, I own a Biocon Pharma that is covered by recall D-0306-2025 from Biocon 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.
