Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Butalbital Recalled by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals Due to Labeling: Not Elsewhere Classified: the controlled substance classification...
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
Butalbital, APAP, Caf 50/325/40 Tablets, packaged in a) 12-count bottles, NDC: 63629-8392-09, barcode 083929152151; b) 60-count bottles, NDC: 63629-8392-03, barcode 083923152614; c) 90-count bottles, NDC:63629-8392-04, barcode 083924152614, Lannett Company Inc; Rx only, Packaged by Bryant Ranch Prepack, Burbank, CA 91504.
Quantity: 119 Bottles
Why Was This Recalled?
Labeling: Not Elsewhere Classified: the controlled substance classification "CIII" is missing on the label
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