Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PrednisoLONE Sodium Phosphate Orally Disintegrating Tablets Recalled by Mylan Pharmaceuticals Inc. Due to CGMP Deviations
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
PrednisoLONE Sodium Phosphate Orally Disintegrating Tablets, 30 mg, Rx Only, 48-count bottle, NDC 00378-4730-22
Quantity: 3,844 48-count bottles
Why Was This Recalled?
CGMP Deviations
Where Was This Sold?
Recalling firm distributed product to wholesalers throughout the United States, including Puerto Rico.
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