Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Spironolactone Tablets Recalled by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals Due to Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone...
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 Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals directly.
Affected Products
Spironolactone Tablets, USP, 25 mg, packaged in: a) 30-count bottles (NDC 63629-1064-01), b) 60-count bottles (NDC 63629-1064-02), c) 90-count bottles (NDC 63629-1064-03), Rx only, Manufactured by: Frontida BioPharm, Inc., Philadelphia, PA 19124 USA, Repackaged by: Bryant Ranch Prepack, Inc., Burbank, CA 91504 USA
Quantity: 35 bottles
Why Was This Recalled?
Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 25 mg may contain spironolactone 50 mg tablets.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report