Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ramipril Capsules USP 2.5 mg Recalled by Lupin Pharmaceuticals Inc. Due to CGMP Deviations: Active pharmaceutical ingredient was sourced from...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Lupin Pharmaceuticals Inc. directly.
Affected Products
Ramipril Capsules USP 2.5 mg, a) 90 count (NDC 68180-589-09), b) 100 count NDC 68180-589-01), and c) 500 count (NDC 68180-589-02) bottles, Rx only, Manufactured for Lupin Pharmaceuticals, Inc., Baltimore, MD, Manufactured by Lupin Limited, Goa, India
Quantity: 112,770 bottles
Why Was This Recalled?
CGMP Deviations: Active pharmaceutical ingredient was sourced from an unapproved vendor
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Lupin Pharmaceuticals Inc.
Lupin Pharmaceuticals Inc. has 119 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report