Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Triamterene and Hydrochlorothiazide Capsules Recalled by Lannett Company Inc. Due to Failed Impurity/Degradation Specifications
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 Lannett Company Inc. directly.
Affected Products
Triamterene and Hydrochlorothiazide Capsules, USP (37.5 mg/25 mg), Rx Only, [100 or 1000 ] Capsules per bottle, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136. NDC 100 Count bottle: 0527-1632-01; NDC 1,000 bottle: 0527-1632-10
Quantity: 20,040 bottles
Why Was This Recalled?
Failed Impurity/Degradation Specifications
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Lannett Company Inc.
Lannett Company Inc. has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report