Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Spironolactone Tablets Recalled by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals Due to Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone...

Date: January 27, 2021
Company: Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
Status: Ongoing
Source: FDA (Drug)

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, 50 mg, packaged in 30-count bottles, Rx only, Manufactured by: Frontida BioPharm, Inc., Philadelphia, PA 19124 USA, Repackaged by: Bryant Ranch Prepack, Inc., Burbank, CA 91504 USA, NDC 63629-1067-01

Quantity: 12 bottles

Why Was This Recalled?

Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 50 mg may contain spironolactone 25 mg tablets.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

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