Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Preferred Pharmaceuticals Recalled by Preferred Pharmaceuticals, Inc Due to CGMP Deviations: Presence of NDMA impurity detected in...
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 Preferred Pharmaceuticals, Inc directly.
Affected Products
Preferred Pharmaceuticals, Inc, Ranitidine Tablets, 300 mg, Rx Only, a) 14 count bottles (NDC: 68788-6382-1), b) 30 count bottles (NDC: 68788-6382-3), c) 90 count bottles (NDC: 68788-6382-9), d) 100 count bottles (NDC: 68788-6382-0)
Quantity: 39,172 tablets
Why Was This Recalled?
CGMP Deviations: Presence of NDMA impurity detected in product.
Where Was This Sold?
This product was distributed to 7 states: AL, AZ, CA, FL, GA, IN, SC
About Preferred Pharmaceuticals, Inc
Preferred Pharmaceuticals, Inc has 10 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report