Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals recalls Spironolactone Tablets, USP, 25 mg, packaged in: a) 30-count bottles (NDC 63629-1064-01), b) 60-count bottles (NDC 63629

Recalled March 24, 2021 · FDA recall D-0303-2021 · Bryant Ranch Prepack, Inc.

Hazard

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

Units

35 bottles

Sold at

Nationwide in the USA

Description

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

Product

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

Manufacturer(s)

Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →