Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Famotidine Tablets USP Recalled by Mylan Pharmaceuticals Inc. Due to Impurities/Degradation Products: Out of specification results for Related...
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 Mylan Pharmaceuticals Inc. directly.
Affected Products
Famotidine Tablets USP, 20 mg, 100 count bottles, Rx Only, Mylan Pharmaceuticals, Inc., Morgantown, WV 26505 U.S.A. NDC 0378-3020-01
Quantity: 31,867 Bottles
Why Was This Recalled?
Impurities/Degradation Products: Out of specification results for Related Compound during routine stability testing.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Mylan Pharmaceuticals Inc.
Mylan Pharmaceuticals Inc. has 71 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report