Lupin Pharmaceuticals recalls Ramipril 10mg capsules due to active pharmaceutical ingredient sourced from an unapproved vendor. This may pose a contamination risk. Consumers should check product details and contact Lupin for guidance.
CGMP Deviations: Active pharmaceutical ingredient was sourced from an unapproved vendor
Lupin Pharmaceuticals is recalling Ramipril 10mg capsules because the active ingredient was sourced from an unapproved vendor, potentially leading to contamination. This recall affects specific packaging sizes and expiration dates. Consumers should check their product details and contact Lupin for further instructions.
The active pharmaceutical ingredient in these capsules was sourced from an unapproved vendor, which could lead to contamination. This contamination might affect the safety and effectiveness of the medication. The exact risk level is not clearly specified in the recall notice.
People who have purchased or received Ramipril 10mg capsules with the specific NDC numbers listed in the recall. Those taking this medication are most at risk if the capsules contain contaminated ingredients.
Check for the product names: Ramipril Capsules USP 10 mg. Look for the NDC numbers 68180-591-09 (90 count), 68180-591-01 (100 count), or 68180-591-02 (500 count). Also, verify the expiration dates and lot numbers listed in the recall notice.
Identify your Ramipril capsules by checking the NDC numbers and expiration dates listed in the recall notice.
The active pharmaceutical ingredient was sourced from an unapproved vendor, which could lead to contamination.
The recall notice does not specify a remedy, so contact Lupin Pharmaceuticals for guidance.
Yes, the recall lists specific expiration dates for each lot, such as 30-Sep-25, 31-Dec-25, and 31-Jul-26.
We’ve drafted a message you can send Lupin to request your refund or repair — edit it as you like.
Subject: Recall D-0054-2025 — Lupin Lupin Hello, I own a Lupin that is covered by recall D-0054-2025 from Lupin. 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.
