Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Amlodipine Besylate Tablets USP Recalled by Lupin Limited Due to CGMP Deviations: finished products manufactured using active pharmaceutical...
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 Limited directly.
Affected Products
Amlodipine Besylate Tablets USP, 2.5mg, 90-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, Manufactured by: Lupin Limited Goa 403 722 INDIA, NDC 68180-750-09
Quantity: 43,536 bottles
Why Was This Recalled?
CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.
Where Was This Sold?
US No recalled product was distributed to any foreign consignees by Lupin.
About Lupin Limited
Lupin Limited has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report