Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ranitidine Tablets Recalled by Dr. Reddy's Laboratories, 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 Dr. Reddy's Laboratories, Inc. directly.
Affected Products
Ranitidine Tablets, USP 150 mg, 190 count bottles (2x95) Tray (Sam's Club) OTC, NDC 150062076 UPC Code 078742089720
Quantity: N/A
Why Was This Recalled?
CGMP Deviations: Presence of NDMA impurity detected in product.
Where Was This Sold?
Product was distributed to major distributors throughout the United States who may have further distributed the product.
About Dr. Reddy's Laboratories, Inc.
Dr. Reddy's Laboratories, Inc. has 163 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report