Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Trandolapril and Verapamil Hydrochloride Extended-Release Tablets 2 mg / 180 mg Recalled by Glenmark Pharmaceuticals Inc., USA Due to Subpotent: Out of Specification for Assay Test at...
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 Glenmark Pharmaceuticals Inc., USA directly.
Affected Products
Trandolapril and Verapamil Hydrochloride Extended-Release Tablets 2 mg / 180 mg, 100-count Bottle, Rx only, Manufactured by: Glenmark Pharmaceuticals Ltd. Colvale -Bardez, Goa 403513, India, Manufactured for Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430, NDC 68462-295-01
Quantity: 1,200 bottles
Why Was This Recalled?
Subpotent: Out of Specification for Assay Test at the 3-month time point.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Glenmark Pharmaceuticals Inc., USA
Glenmark Pharmaceuticals Inc., USA has 139 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report