Lupin Pharmaceuticals recalls 2.5mg Ramipril capsules due to active pharmaceutical ingredient sourced from an unapproved vendor. This may affect safety for users. Check NDC codes and expiration dates for affected lots.
CGMP Deviations: Active pharmaceutical ingredient was sourced from an unapproved vendor
Lupin Pharmaceuticals is recalling specific lots of Ramipril 2.5mg capsules because the active ingredient was sourced from an unapproved vendor. This could pose a safety risk to users who take the medication.
The active pharmaceutical ingredient in these capsules was sourced from an unapproved vendor, which may lead to inconsistent quality or safety issues. This could affect the medication's effectiveness or cause adverse reactions in users.
People who have the recalled lots of Ramipril capsules (NDC 68180-589-09, 68180-589-01, or 68180-589-02) are affected. Those taking blood pressure medication are most at risk.
Check the NDC code on the bottle (68180-589-09, 68180-589-01, or 68180-589-02) and expiration date. The recalled lots have specific expiration dates listed in the recall notice.
Identify the NDC code and expiration date on your Ramipril capsules to see if they match the recalled lots.
The active pharmaceutical ingredient was sourced from an unapproved vendor, which may lead to inconsistent quality or safety issues.
The recall notice does not specify a remedy, so check the product details to see if it matches the recalled lots.
The recall indicates a potential safety risk due to the unapproved vendor, but the exact risk level is not specified in the notice.
We’ve drafted a message you can send Lupin Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0052-2025 — Lupin Pharmaceuticals Lupin Pharmaceuticals Hello, I own a Lupin Pharmaceuticals that is covered by recall D-0052-2025 from Lupin Pharmaceuticals. 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.
